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  • Hiv/aids In Egypt Wikipedia
    External links [ edit ] In Egypt, Battling the Stigma of HIV Catholic Relief Services Video and Photography Material related to HIV/AIDS in Egypt: Sotna Pilot Children's Show on HIV/AIDS produced by UNICEF Egypt v t e HIV/AIDS in Africa Sovereign states Algeria Angola Benin Botswana Burkina Faso Burundi Cameroon Cape Verde (Cabo Verde) Central African Republic Chad Comoros Democratic Republic of the Congo Republic of the Congo Djibouti Egypt Equatorial Guinea Eritrea Eswatini (Swaziland) Ethiopia Gabon The Gambia Ghana Guinea Guinea-Bissau Ivory Coast (Côte d'Ivoire) Kenya Lesotho Liberia Libya Madagascar Malawi Mali Mauritania Mauritius Morocco Mozambique Namibia Niger Nigeria Rwanda São Tomé and Príncipe Senegal Seychelles Sierra Leone Somalia South Africa South Sudan Sudan Tanzania Togo Tunisia Uganda Zambia Zimbabwe States with limited recognition Sahrawi Arab Democratic Republic Somaliland Dependencies and other territories Canary Islands / Ceuta / Melilla (Spain) Madeira (Portugal) Mayotte / Réunion (France) Saint Helena / Ascension Island / Tristan da Cunha (United Kingdom) v t e HIV/AIDS in Asia Sovereign states Afghanistan Armenia Azerbaijan Bahrain Bangladesh Bhutan Brunei Cambodia China Cyprus East Timor (Timor-Leste) Egypt Georgia India Indonesia Iran Iraq Israel Japan Jordan Kazakhstan North Korea South Korea Kuwait Kyrgyzstan Laos Lebanon Malaysia Maldives Mongolia Myanmar Nepal Oman Pakistan Philippines Qatar Russia Saudi Arabia Singapore Sri Lanka Syria Tajikistan Thailand Turkey Turkmenistan United Arab Emirates Uzbekistan Vietnam Yemen States with limited recognition Abkhazia Artsakh Northern Cyprus Palestine South Ossetia Taiwan Dependencies and other territories British Indian Ocean Territory Christmas Island Cocos (Keeling) Islands Hong Kong Macau Book Category Asia portal v t e HIV / AIDS topics HIV/AIDS HIV HIV Lentivirus structure and genome subtypes CDC classification disease progression rates HIV/AIDS diagnosis management pathophysiology prevention research vaccination PrEP WHO disease staging system for HIV infection and disease Children Teens / Adults Countries by AIDS prevalence rate Conditions Signs and symptoms AIDS-defining clinical condition Diffuse infiltrative lymphocytosis syndrome Lipodystrophy Nephropathy Neurocognitive disorders Pruritus Superinfection Tuberculosis co-infection HIV Drug Resistance Database Innate resistance to HIV Serostatus HIV-positive people Nutrition Pregnancy History History Epidemiology Multiple sex partners Timeline AIDS Museum Timothy Ray Brown Women and HIV/AIDS Social AIDS orphan Catholic Church and HIV/AIDS Circumcision and HIV Criminal transmission Discrimination against people Economic impact Cost of treatment HIV-affected community HIV/AIDS activism HIV/AIDS denialism Red ribbon Safe sex Sex education List of HIV-positive people People With AIDS Self-Empowerment Movement HIV/AIDS in the porn industry Culture Discredited HIV/AIDS origins theories International AIDS Conference International AIDS Society Joint United Nations Programme on HIV/AIDS (UNAIDS) Media portrayal of HIV/AIDS Misconceptions about HIV/AIDS President's Emergency Plan for AIDS Relief (PEPFAR) The SING Campaign Solidays Treatment Action Campaign World AIDS Day YAA/Youthforce "Free Me" Larry Kramer Gay Men's Health Crisis ACT UP Silence=Death Project HIV/AIDS pandemic by region / country Africa Angola Benin Botswana Democratic Republic of the Congo Egypt Eswatini Ethiopia Ghana Guinea Côte d'Ivoire (Ivory Coast) Kenya Lesotho Madagascar Malawi Mali Mozambique Namibia Niger Nigeria Rwanda Senegal Tanzania South Africa Uganda Zambia Zimbabwe North America Canada Mexico El Salvador Guatemala Honduras Nicaragua United States New York City Caribbean Haiti Jamaica Dominican Republic South America Bolivia Brazil Colombia Guyana Peru Asia Afghanistan Armenia Azerbaijan Bahrain Bangladesh Bhutan Cambodia China (PRC) ( Yunnan ) East Timor India Indonesia Iran Iraq Japan Jordan North Korea Laos Malaysia Myanmar (Burma) Nepal Pakistan Philippines Saudi Arabia Sri Lanka Taiwan (ROC) Thailand United Arab Emirates Turkey Vietnam Europe United Kingdom Russia Ukraine Oceania Australia New Zealand Papua New Guinea List of countries by HIV/AIDS adult prevalence rate List of HIV/AIDS cases and deaths registered by region
  • Melanoma, Uveal OMIM
    See also 614327 for a tumor predisposition syndrome that may include the development of uveal melanoma and is caused by germline mutation in the BAP1 gene (603089) on chromosome 3p21.
    CYSLTR2, GNA11, GNAQ, SF3B1, BAP1, LDLRAD4, DDR2, BRAF, TP53, BCL2, MAPK8, PERP, BAG3, HAT1, VEGFA, TYRP1, PIK3CD, PLXNA2, PIK3CG, PIK3CB, PIK3CA, MMP2, MARCKS, IFNA2, FGF2, KYAT1, OCM
    • Melanoma, Uveal, Susceptibility To, 2 OMIM
      Uveal melanoma (155720) is the most common primary intraocular malignancy. Monosomy 3, which is an unusual finding in most tumors, is present in approximately 50% of uveal melanomas and is significantly correlated with metastatic disease. To obtain positional information on putative tumor suppressor genes on chromosome 3, Tschentscher et al. (2001) investigated tumors from 333 patients by comparative genomic hybridization, microsatellite analysis, or conventional karyotype analysis. A partial deletion of the long arm was found in 8 tumors, and the smallest region of deletion overlap (SRO) spanned 3q24-q26. They found 6 tumors with a partial deletion of the short arm and defined a second SRO of about 2.5 Mb in 3p25.
    • Melanoma, Uveal, Susceptibility To, 1 OMIM
      Uveal melanoma (155720) is the most common primary intraocular malignancy. Monosomy 3, which is an unusual finding in most tumors, is present in approximately 50% of uveal melanomas and is significantly correlated with metastatic disease. To obtain positional information on putative tumor suppressor genes on chromosome 3, Tschentscher et al. (2001) investigated tumors from 333 patients by comparative genomic hybridization, microsatellite analysis, or conventional karyotype analysis. A partial deletion of the long arm was found in 8 tumors, and the smallest region of deletion overlap (SRO) spanned 3q24-q26. They found 6 tumors with a partial deletion of the short arm and defined a second SRO of about 2.5 Mb in 3p25.
  • Multiple Sclerosis, Susceptibility To OMIM
    Kumpfel et al. (2008) identified 20 patients with MS who carried a heterozygous variant (R92Q) in the TNFRSF1A gene (191190) and had clinical features consistent with late-onset of the tumor necrosis factor receptor 1-associated periodic syndrome (TRAPS; 142680), including myalgias, arthralgias, headache, fatigue, and skin rashes. ... Disanto et al. (2011) found that 64 (24%) of 266 children with an initial attack of demyelination (acquired demyelinating syndrome, ADS) met criteria for a diagnosis of MS during a mean follow-up of 3.2 years.
    • Multiple Sclerosis MedlinePlus
      Multiple sclerosis is a condition characterized by areas of damage (lesions) on the brain and spinal cord . These lesions are associated with destruction of the covering that protects nerves and promotes the efficient transmission of nerve impulses (the myelin sheath ) and damage to nerve cells. Multiple sclerosis is considered an autoimmune disorder; autoimmune disorders occur when the immune system malfunctions and attacks the body's own tissues and organs, in this case tissues of the nervous system. Multiple sclerosis usually begins in early adulthood, between ages 20 and 40. The symptoms vary widely, and affected individuals can experience one or more effects of nervous system damage.
  • Angiotensin I-Converting Enzyme OMIM
    Catarsi et al. (2005) studied 227 Italian nephrotic syndrome patients in whom hypertension was the major side effect of treatment by cyclosporine A (CsA).
  • Parkinson Disease, Late-Onset OMIM
    However, parkinsonism without Lewy bodies characterizes progressive supranuclear palsy (PSP; 601104), frontotemporal dementia with parkinsonism (600274), autosomal dominant (128230) and recessive (605407) forms of Segawa syndrome, X-linked recessive Filipino type of dystonia (314250), multiple systems atrophy, and cerebrovascular disease.
    GBA, MAPT, ATXN2, TBP, GLUD2, PRKN, DNAJC13, NR4A2, TMEM230, ADH1C, SNCAIP, ATXN8OS, LRRK2, ATXN3, SNCA, LRP2, MCF2L, CRP, ALB, VPS35, EEF1A2, PINK1, SLC6A3, LAMC2, CSF2, TPO, BDNF, COMT, APOE, CYP2D6, IL6, TGFB1, MAOB, ADIPOQ, PTH, GCG, VEGFA, GIGYF2, SLC6A4, STXBP3, GSTM1, TOMM40, TET2, RIDA, BPIFA2, HFE, PSPH, PSPN, GBAP1, HTR2A, SOST, IL1B, VCAM1, HAMP, YWHAE, LEP, PARK10, CCN2, TARDBP, KL, DRD2, DRD3, ASXL1, CAT, NLRP3, MSMB, ATP13A2, PLA2G6, SMPD1, SF3B1, REN, PAFAH1B1, REG1A, HTRA2, APOB, UCP2, VDR, USP24, WNT2, WNT1, WWC1, ACSBG1, SARM1, PARK7, PPARGC1A, NFAT5, WASF2, FGF23, HERPUD1, B3GALT4, CARTPT, PPIG, CLDN1, TRAP1, ADA, PART1, TMEM98, CNDP1, LINGO1, MIDN, TPH2, TMEM132E, SLCO6A1, CDAN1, GLIS1, C9orf72, STH, SLC41A1, CLEC4D, GSTK1, MIR107, MIR137, MIR184, MIR21, MIR221, MIR302C, CCR2, ZGLP1, PARK16, BED, C19orf12, SETD7, COL18A1, PLEKHO1, SLC17A5, GREM1, LAT, PDCD4, REM1, CD274, ITSN2, TRAT1, TNFRSF1A, CHCHD2, TNFRSF12A, EHMT1, PRRX2, SCLY, VPS29, USP40, RHOT1, CYP20A1, ANO3, MARCHF7, RAPH1, LRRK1, NTM, SFSWAP, TNF, DRD5, ELAVL4, ELK3, EPHB1, ERBB2, EZH2, F3, FGF2, FH, FMR1, FN1, FRA6E, GALC, GAPDH, GCH1, GDNF, GLA, GLP1R, GRIN2B, HMOX1, FOXA1, HSPA1A, EIF4G1, DRD1, HSPA2, DPYD, AGER, AHSG, AKT1, ALDH2, ANGPT2, APOA1, APOD, AR, ARSA, AVP, BCHE, CEACAM1, BRAF, C1QC, CA12, CD34, CD68, CDKN2B, CHM, COL1A1, CLDN7, HSPA1B, IFNA1, TLR4, PPARG, PTGDS, PTGS2, RAD23A, PRPH2, ROM1, S100B, CCL2, SGCA, ST3GAL2, SKP1, SLC6A2, SLC18A2, SMN1, SMN2, SPARC, SPTBN1, SYP, TAL1, PRDX2, TGFBR1, TH, MAPK3, PON1, IFNA13, ABCB1, IL2RA, IL10, KRT7, LPA, LY6E, CD46, NR3C2, MMP1, MMP3, MMP9, MTHFR, NEFL, NGFR, NOS3, SLC11A2, OGG1, P2RY6, PAEP, PARK3, PECAM1, PENK, LOC107987479
  • Hfe Hemochromatosis GeneReviews
    ., beta-thalassemia, sickle cell disease, hereditary sideroblastic anemia, pyruvate kinase deficiency, hereditary spherocytosis, myelodysplastic syndrome with refractory anemia). Iron absorption is increased in some subtypes of heritable anemia, especially severe beta-thalassemia and hereditary sideroblastic anemia.
    HFE, HJV, BMP2, HAMP, TF, TFR2, TFRC, HLA-A, SLC40A1, HLA-H, TMPRSS6, BMP6, SLC11A2, TNF, CP, CYBRD1, APOE, HLA-F, HLA-B, GSTP1, GNPAT, EPO, FTL, UBE2D1, SUCNR1, B2M, COX8A, TLR4, ZKSCAN8, PCSK7, ADIPOQ, FADS2, TP53, UROD, NAT2, PIEZO1, HEPH, TRIM31, NUP42, PPP1R11, BCO1, EAF2, TNMD, SLC46A1, BTBD9, GAB3, MCIDAS, LINC01194, HPGDS, MMP1, SOD1, GABPA, ALAD, ALB, ALDH2, ARNTL, ATP7B, CALR, CFTR, CTNNB1, CYLD, F5, FOXC2, FXN, GAST, FUT2, GAPDH, UBL3, GC, GNRH1, HP, IGFALS, IGHG3, IL6, SMAD1, SMAD7, MDM2, AGTR1, NFE2L2, NMBR, PGF, SERPINA1, MFT2
    • Symptomatic Form Of Hemochromatosis Type 1 Orphanet
      Symptomatic form of hemochromatosis type 1 is a rare, hereditary hemochromatosis characterized by inappropriately regulated intestinal iron absorption which leads to excessive iron storage in various organs and manifests with a wide range of signs and symptoms, including abdominal pain, weakness, lethargy, weight loss, elevated serum aminotransferase levels, increase in skin pigmentation, and/or arthropathy in the metacarpophalangeal joints. Other commonly associated manifestations include hepatomegaly, cirrhosis, liver fibrosis, hepatocellular carcinoma, restrictive cardiomyopathy and/or diabetes mellitus.
    • Hemochromatosis, Type 1 OMIM
      A number sign (#) is used with this entry because hemochromatosis type 1 (HFE1) is caused by homozygous or compound heterozygous mutation in the HFE gene (613609) on chromosome 6p22. Description Hereditary hemochromatosis is an autosomal recessive disorder of iron metabolism wherein the body accumulates excess iron (summary by Feder et al., 1996). Excess iron is deposited in a variety of organs leading to their failure, and resulting in serious illnesses including cirrhosis, hepatomas, diabetes, cardiomyopathy, arthritis, and hypogonadotropic hypogonadism. Severe effects of the disease usually do not appear until after decades of progressive iron loading. Removal of excess iron by therapeutic phlebotomy decreases morbidity and mortality if instituted early in the course of the disease.
    • Hereditary Hemochromatosis MedlinePlus
      Hereditary hemochromatosis is a disorder that causes the body to absorb too much iron from the diet. The excess iron is stored in the body's tissues and organs, particularly the skin, heart, liver , pancreas , and joints. Because humans cannot increase the excretion of iron, excess iron can overload and eventually damage tissues and organs. For this reason, hereditary hemochromatosis is also called an iron overload disorder. Early symptoms of hereditary hemochromatosis may include extreme tiredness (fatigue), joint pain, abdominal pain, weight loss, and loss of sex drive.
  • Leukoencephalopathy With Neuroaxonal Spheroids Wikipedia
    "Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia Can Present as Frontotemporal Dementia Syndrome" . Dementia and Geriatric Cognitive Disorders . 32 (2): 150–158. doi : 10.1159/000331422 .
  • Source Amnesia Wikipedia
    This has seen to occur in the music industry and has the implication of copyright infringement over songs, as well as in the formation of scientific research ideas. [41] See also [ edit ] Context-dependent memory Memory distrust syndrome Sleeper effect References [ edit ] ^ a b Schacter, D.L., Harbluk, J.L., and McLachlen, D.R. (1984).
  • Abortion Wikipedia
    Taussig wrote that a cause of increasing mortality during the years of illegality in the U.S. was that With each decade of the past fifty years the actual and proportionate frequency of this accident [perforation of the uterus] has increased, due, first, to the increase in the number of instrumentally induced abortions; second, to the proportionate increase in abortions handled by doctors as against those handled by midwives; and, third, to the prevailing tendency to use instruments instead of the finger in emptying the uterus. [114] : 223 Mental health Main article: Abortion and mental health Current evidence finds no relationship between most induced abortions and mental health problems [14] [115] other than those expected for any unwanted pregnancy. [116] A report by the American Psychological Association concluded that a woman's first abortion is not a threat to mental health when carried out in the first trimester, with such women no more likely to have mental-health problems than those carrying an unwanted pregnancy to term; the mental-health outcome of a woman's second or greater abortion is less certain. [116] [117] Some older reviews concluded that abortion was associated with an increased risk of psychological problems; [118] however, they did not use an appropriate control group. [115] Although some studies show negative mental-health outcomes in women who choose abortions after the first trimester because of fetal abnormalities, [119] more rigorous research would be needed to show this conclusively. [120] Some proposed negative psychological effects of abortion have been referred to by anti-abortion advocates as a separate condition called " post-abortion syndrome ", but this is not recognized by medical or psychological professionals in the United States. [121] A long term-study among US women found that about 99% of women felt that they made the right decision five years after they had an abortion.
  • Inflammation Wikipedia
    Non-immune diseases with causal origins in inflammatory processes include cancer, atherosclerosis , and ischemic heart disease . [10] Examples of disorders associated with inflammation include: Acne vulgaris Asthma Autoimmune diseases Autoinflammatory diseases Celiac disease Chronic prostatitis Colitis Diverticulitis Familial Mediterranean Fever Glomerulonephritis Hidradenitis suppurativa Hypersensitivities Inflammatory bowel diseases Interstitial cystitis Lichen planus Mast Cell Activation Syndrome Mastocytosis Otitis Pelvic inflammatory disease pneumonia Reperfusion injury Rheumatic fever Rheumatoid arthritis Rhinitis Sarcoidosis Transplant rejection Vasculitis Atherosclerosis [ edit ] Main article: Atherosclerosis Atherosclerosis, formerly considered a bland lipid storage disease, actually involves an ongoing inflammatory response. ... Elevation in markers of inflammation predicts outcomes of patients with acute coronary syndromes, independently of myocardial damage. ... They may occur in conjunction with other immune disorders, such as systemic sclerosis , and include dermatomyositis , polymyositis , and inclusion body myositis . [10] Leukocyte defects [ edit ] Due to the central role of leukocytes in the development and propagation of inflammation, defects in leukocyte functionality often result in a decreased capacity for inflammatory defense with subsequent vulnerability to infection. [10] Dysfunctional leukocytes may be unable to correctly bind to blood vessels due to surface receptor mutations, digest bacteria ( Chédiak–Higashi syndrome ), or produce microbicides ( chronic granulomatous disease ). ... When inflammation overwhelms the host, systemic inflammatory response syndrome is diagnosed. When it is due to infection , the term sepsis is applied, with the terms bacteremia being applied specifically for bacterial sepsis and viremia specifically to viral sepsis.
    TNF, CRP, PTGS2, IL6, IL1B, TLR2, MIF, ICAM1, IL10, CCL2, BDNF, PPARG, TRPV1, IL1RN, TAC1, FGF2, PTGES, BDKRB2, NGF, CALCA, PTGER4, CXCL8, TGFB1, LEP, IFNG, ADIPOQ, IL17A, HMOX1, TLR4, F2RL1, HMGB1, MMP9, VEGFA, MPO, SOD1, PARP1, SCGB1A1, UCN, TIMP1, IL13, LTB4R, BDKRB1, CSF2, PPARA, AGER, AHR, TLR9, PLAUR, NOS2, LCN2, LTF, NLRP3, TNFRSF11B, CXCR3, APOA1, PROCR, IDO1, MMP2, TNFSF15, F2R, TSLP, EGR1, EIF4EBP1, EPO, CCL4, CCL11, CCL3, MYD88, MVK, EFNB1, EDN1, RORC, PTPN1, COL2A1, JAK2, OXT, IRF7, CRHR2, ABCB4, CHRNA4, CHRNB2, NPPB, SLC22A5, CLN6, GATA3, MASP2, DUSP10, TREX1, ANGPT1, IL17RA, TBX21, GAL, AKT1, SELENOS, CXCL2, AGT, UCN3, IFNL3, MIR21, MIR217, MIR22, ASIC1, ASIC2, MIR34A, GALNS, SH2B3, NR1H4, WDR1, STAT3, SULT2B1, TF, TFRC, TGFA, CD3E, CCK, TNFAIP3, TP73, TSC2, ZFP36, IL1A, KYNU, TRPA1, ASIC3, ATP7B, PLAA, STS, CASP1, IL15, CXCL1, ANXA1, TLR6, CCL5, F11R, KLK1, APOA4, ABCB1, MUC2, TACR3, ACSL6, HP, PDPN, PDE5A, NPFF, TFAM, SDC1, TACR1, NPY5R, CXCR2, S100A8, PLA2G4A, PIK3CG, PCSK2, PCSK1, OPRM1, KCNK2, NTRK2, SPINK1, A2M, SERPINC1, F3, ACSL4, ACSL3, CCR5, AIF1, FGG, CDK5, CX3CR1, CYP1A1, CAMK2A, ADORA1, EGFR, ALOX5, SERPINA3, ALOX5AP, MTOR, CCL20, IL23A, NFKB1, CX3CL1, IL18, ELANE, PRTN3, PROC, THBS1, CD40, SERPINE1, C5, MMP3, HSPA4, NOS3, RELA, CCR6, SPP1, NOD1, PLAU, RETN, CNR2, CXCL10, ADM, NOD2, IL33, MAPK14, S100B, SAA1, TNFSF13B, CEACAM1, NFE2L2, CRYAB, DEFB4A, PGF, APP, S100A9, CST3, TNFSF18, POMC, TNFSF14, NTF3, MT2A, TNFRSF1A, BMP4, TNFSF10, CCL21, TNFAIP6, FOXP3, CFTR, HGF, TP53, TPSAB1, VEGFC, EOLA1, CD40LG, CD44, FGF1, IL25, HAMP, KNG1, C1QBP, VWF, MBL2, SELPLG, SLC15A1, NR3C2, GHRL, SELP, C3AR1, C3, IL32, VCAM1, CD83, TNFSF12, C4A, TYROBP, C4B, SOCS1, CD163, CYP7B1, TNFRSF17, BST1, VEGFB, BSG, SLC28A2, TNFSF13, SOCS3, VIP, SERPING1, VTN, PLA2G6, BPI, APLN, TNFRSF18, YWHAG, TFPI2, YWHAH, DAP3, MADCAM1, GTF2A1, NTN1, AQP7, ADA2, TREM1, DLL4, AHSG, AGTR1, APOM, SCUBE2, CXCL16, SLC28A3, RASL11B, ADIPOR2, TREML2, SCUBE1, SETD7, ADRB3, LACRT, TNFRSF13C, APOA5, CD200R1, CLEC12A, IL27, PYDC1, ADCYAP1, PLA2G4D, NLRP10, ENPP7, ADAR, ADA, ACP5, TNFRSF12A, KCNK9, TLR7, APCS, CXCL14, AQP4, AQP3, FASLG, FAS, NAMPT, CCL26, KLF2, APOD, TXNIP, AQP8, BIRC5, LIAS, PTGDR2, ADIPOR1, ANGPT2, NCOA6, ANG, SIRT1, TNFRSF13B, BIN1, PRDX5, EHF, IL36A, PADI1, ALPL, IL20, IL22, LILRB1, CHI3L1, C5AR1, MMP10, F11, LIF, LIMK1, F7, SMAD3, SMAD7, MAZ, MEFV, CD99, MME, MMP1, F2, ELF3, CD200, FCAR, MUC1, EGF, DSG2, NCAM1, DMBT1, NAT1, NPPC, DEFA3, NTF4, DEFA1, DDT, CYP19A1, CYP2C19, KCNK3, FCGR1A, CACNA1C, FPR2, NRG1, HIF1A, NR3C1, GRN, GH1, HRH1, HSP90AA1, HSPD1, GCH1, ACKR1, IGF1, GAST, IL1RAP, IL4R, ITIH2, FN1, FLT3LG, FLT1, FKBP4, IL12A, IL12B, FGF7, TNFRSF9, FCGR3A, IRF1, FCGR2A, ITGA1, ITGAL, PDGFA, PDGFB, PDGFRB, SPRR1B, CCR8, CCR7, CCL13, CCL18, CCL19, CXCL6, CXCL11, CLU, CXCL12, SELE, SFTPD, GZMA, CDKN1A, STC1, PECAM1, CDH1, CD68, CD48, CD47, CD38, CD28, TGM2, THBD, CAT, TIMP4, CAMP, TLR3, TMSB4X, ACKR2, CCL1, SERPINB4, SERPINB3, SERPINF1, PF4, PGR, CTSG, CTSB, PHB, SERPINA1, PIGF, CTNNB1, PLAT, CSF1, PLCB3, PLP1, PON1, PRKAA1, PRKCD, PRSS3, PTEN, CRH, CPB2, PTN, CNTF, PTX3, RET, S100A7, CNR1, S100A12, CARD17
  • Subarachnoid Hemorrhage Wikipedia
    This headache often pulsates towards the occiput (the back of the head). [7] About one-third of people have no symptoms apart from the characteristic headache, and about one in ten people who seek medical care with this symptom are later diagnosed with a subarachnoid hemorrhage. [4] Vomiting may be present, and 1 in 14 have seizures . [4] Confusion , decreased level of consciousness or coma may be present, as may neck stiffness and other signs of meningism . [4] Neck stiffness usually presents six hours after initial onset of SAH. [8] Isolated dilation of a pupil and loss of the pupillary light reflex may reflect brain herniation as a result of rising intracranial pressure (pressure inside the skull). [4] Intraocular hemorrhage (bleeding into the eyeball) may occur in response to the raised pressure: subhyaloid hemorrhage (bleeding under the hyaloid membrane , which envelops the vitreous body of the eye) and vitreous hemorrhage may be visible on fundoscopy . This is known as Terson syndrome (occurring in 3–13 percent of cases) and is more common in more severe SAH. [9] Oculomotor nerve abnormalities (affected eye looking downward and outward and inability to lift the eyelid on the same side ) or palsy (loss of movement) may indicate bleeding from the posterior communicating artery . [4] [7] Seizures are more common if the hemorrhage is from an aneurysm; it is otherwise difficult to predict the site and origin of the hemorrhage from the symptoms. [4] SAH in a person known to have seizures is often diagnostic of a cerebral arteriovenous malformation . [7] The combination of intracerebral hemorrhage and raised intracranial pressure (if present) leads to a "sympathetic surge", i.e. over-activation of the sympathetic system. ... "A systematic review of Terson's syndrome: frequency and prognosis after subarachnoid haemorrhage" .
    CASP3, EDN1, PPARG, NTN1, THSD1, UNC5B, NOS2, EDNRB, NOS3, ADORA1, MMP9, TLR4, TNF, BCL2, TNC, NFE2L2, HMOX1, AGER, BECN1, CYBB, CASP9, ABCC8, TRPM4, ICAM1, STAT3, GSK3B, NGB, TJP1, MMP2, NTRK2, HTR1B, HSPD1, MMP13, GLI1, TACR1, SHH, KCNJ10, NQO1, PRKN, ESR1, PTCH1, NLK, CCL20, HIF1A, CXCL1, BNIP3, HCN1, C3, ELN, ENG, ITGB3, COL3A1, MYLK, PRKG1, TGFB2, PIK3CB, PIK3CA, F10, FBN1, TGFBR1, ACSM3, TGFB3, MFAP5, TGFBR2, TGFBR3, ACTA2, ACVRL1, CD109, NLRP3, ANGPTL6, DOCK8, HP, HMGB1, APOE, IL6, ITGA2, ITGA2B, GP1BB, GP1BA, LAMC2, LOX, SMAD3, SMAD4, GDF2, PIK3CD, MAT2A, FOXE3, MYH11, CRP, CSF2, PIK3CG, IL1B, MAPK1, SIRT1, BDNF, ALB, ACE, COL4A2, MPO, SPP1, CEBPZ, RIPK3, MAPK8, AQP4, VEGFA, EPHB2, POSTN, MAPK14, S100B, TXNIP, OR10A4, XYLT2, LGALS3, CALCA, F3, ADAMTS13, IL1A, TP53, MPRIP, GABPA, SOD1, JAK2, MST1, IL10, POLDIP2, SIRT3, TREM1, RNF19A, APLN, AHSA1, DNM1L, GRAP2, RIPK1, AIMP2, MIF, VWF, VCAM1, MYD88, UGCG, SERPINE1, S100A12, RYR1, PDGFRB, REN, SOD2, SERPINA3, AVP, GCLC, AGTR1, EPO, CBS, CRK, GRM1, GFAP, AKT1, ROCK2, AGT, TMBIM6, CTNNB1, SARDH, CX3CR1, MTOR, PKD1, ATF4, CASP1, MOK, ERBB4, CD163, TBL1X, P2RX7, HAMP, NPY, SORD, FCN1, AIF1, NEFL, PTK2B, UTS2, PCSK1, RALBP1, SDS, DAPK3, F2, SDHB, PHB2, DDIT3, IL17A, ENO2, DAPK2, EGFR, SMUG1, DENR, VDR, MAP2K1, MIR502, MIR30A, OCLN, UTRN, UQCRFS1, CBSL, TTR, PRKAB1, PRKAA2, HSPB3, ABO, GLP1R, PRKAA1, TNFRSF1A, CRMP1, CLDN5, AQP1, C20orf181, MASP2, NGEF, PANX1, BIRC2, KDM6B, HPSE, TARDBP, BGN, XIAP, APP, ATF6, MAPK8IP3, HSP90AA1, TSPO, ERLIN1, HAP1, SELENBP1, DLK1, TNFSF12, CD36, MBTPS1, S1PR4, PEA15, CD38, FCN3, PLA2G6, ST8SIA2, CD44, CD68, PLA2G7, RPS6KA5, KLF4, ADIPOQ, C5AR1, C5, YAP1, IRF9, APBB3, NET1, SLC25A15, CAST, CASP8, APPL1, KEAP1, PCLAF, HDAC4, CLOCK, ATG5, SRA1, SIRT6, ANXA7, SLA2, CPP, TSPAN33, SCARA5, BTBD8, ADM, COPD, ADRB1, MLKL, GPBAR1, LYPD4, ROMO1, ADRB2, HSPB6, NEXN, IL33, RIOX2, ZGPAT, MIR132, MIR143, MIR145, MIR532, RN7SL263P, MIR4793, MIR1297, H3P36, MIR675, CCR2, MIR630, ECSCR, MIR15A, MIR324, MIR24-1, MIR221, MIR22, MIR21, MIR206, MIR183, POLDIP3, RAB34, CLEC4E, TRAPPC9, MOCOS, ALDH2, PDP1, DDIT4, CCHCR1, TERF2IP, ALOX15, ANGPT1, CXCR4, PRRX2, NRN1, TLR7, NOX4, SETD2, SGSM3, RABGEF1, INTU, AGGF1, PPP6R3, MEG3, WNK1, APLNR, ITM2C, PPP1R2C, RIOX1, MMEL1, MAPKAP1, WNK2, PINK1, AKT2, GORASP1, SOX17, RXFP1, ACE2, MRS2, PELI1, ZC4H2, MANF, TRAF2, MAP3K12, FPR2, MTHFR, FGFR3, MSR1, MRC1, FOXO3, MPG, MNT, MMP12, FGFR1, MMP10, MMP7, MMP3, NR5A2, MMP1, CXCL9, GAP43, MYC, FGF13, PLAT, OLR1, PLA2G1B, ERN1, F2R, PDE4A, PCMT1, FCGR3A, PRDX1, OCA2, FGF2, NUCB2, FCGR3B, NPPB, NOTCH1, FDPS, FES, NEFH, MET, MAP3K5, MEFV, HLA-A, IL18, CXCL3, CXCL8, IL7, IL6R, NRG1, IL1RN, HPX, SMCP, CCN1, IGF1, IFNA13, IFNA1, HSPA4, HSPA5, HSPB1, CXCL10, IRAK1, GRIN2B, GRIA1, MC1R, MBP, KAT2A, MAS1, MARS1, MAP2, GJA1, LRPAP1, LIMK1, LCN2, GLS, LAMP1, GPER1, GPT, ITPR3, PLA2G2A, PLCD1, SLC30A3, CTSG, TLR2, CRYGD, TIMP3, TIMP1, THBD, TH, CCN2, CYP3A4, CRY2, TFPI, PRDX2, TAT, MAP3K7, SYT1, SYN1, DBH, TLR3, TM7SF2, PLXNB1, CLU, ZMYM2, ZFP36, WNT1, CEBPA, VTN, VIP, CHRM3, VASP, TNNI3, CLDN3, UCP3, UCP2, TRH, TRAF6, HSPB2, NR2C2, DBP, SSRP1, SPTAN1, PTEN, EGF, RELA, RAP1A, PTK2, PTGS2, PTGS1, PTGER4, MASP1, ECI1, MAP2K7, EGR1, MAPK3, ABCA1, PTPA, EPHA4, PRRX1, TRIM27, BRD2, RNPEP, ROCK1, DCX, SLC9A1, SLC2A1, DECR1, SHBG, SELENOP, SELP, CCL13, CCL2, HBEGF, E2F1, S1PR1, S100A1, EDNRA, ROS1, LINC02605
    • Subarachnoid Hemorrhage Mayo Clinic
      Overview A subarachnoid hemorrhage is bleeding in the space between the brain and the surrounding membrane (subarachnoid space). The primary symptom is a sudden, severe headache. Some people describe it as the worst headache they have ever felt. Along with having a headache, some people may experience: Nausea Vomiting Stiff neck Problems with vision Brief loss of consciousness Bleeding usually happens when an irregular bulge in a blood vessel (aneurysm) bursts in the brain. Sometimes, bleeding is caused by trauma, a tangle of blood vessels in the brain (arteriovenous malformation), or other blood vessel or health problems. Untreated, a subarachnoid hemorrhage can lead to permanent brain damage or death.
  • Abortion In The United Kingdom Wikipedia
    Prominent campaign groups which are supportive of a conservative policy include: Both Lives Matter Cherish all the Children Equally Christian Action, Research & Education (CARE) Don't Screen Us Out (in relation to children with Down's Syndrome) Evangelical Alliance Precious Life Society for the Protection of Unborn Children (SPUC) Prominent campaign groups which are supportive of a liberal policy include: Alliance for Choice Amnesty International Belfast Feminist Network British Pregnancy Advisory Service (BPAS) Brook Clinic Family Planning Association (FPA) Marie Stopes Humanists UK This section needs to be updated .
  • Hiv/aids In The United Kingdom Wikipedia
    . ^ https://www.bbc.co.uk/news/health-51897856 v t e HIV/AIDS in Europe Sovereign states Albania Andorra Armenia Austria Azerbaijan Belarus Belgium Bosnia and Herzegovina Bulgaria Croatia Cyprus Czech Republic Denmark Estonia Finland France Georgia Germany Greece Hungary Iceland Ireland Italy Kazakhstan Latvia Liechtenstein Lithuania Luxembourg Malta Moldova Monaco Montenegro Netherlands North Macedonia Norway Poland Portugal Romania Russia San Marino Serbia Slovakia Slovenia Spain Sweden Switzerland Turkey Ukraine United Kingdom States with limited recognition Abkhazia Artsakh Kosovo Northern Cyprus South Ossetia Transnistria Dependencies and other entities Åland Faroe Islands Gibraltar Guernsey Isle of Man Jersey Svalbard v t e HIV / AIDS topics HIV/AIDS HIV HIV Lentivirus structure and genome subtypes CDC classification disease progression rates HIV/AIDS diagnosis management pathophysiology prevention research vaccination PrEP WHO disease staging system for HIV infection and disease Children Teens / Adults Countries by AIDS prevalence rate Conditions Signs and symptoms AIDS-defining clinical condition Diffuse infiltrative lymphocytosis syndrome Lipodystrophy Nephropathy Neurocognitive disorders Pruritus Superinfection Tuberculosis co-infection HIV Drug Resistance Database Innate resistance to HIV Serostatus HIV-positive people Nutrition Pregnancy History History Epidemiology Multiple sex partners Timeline AIDS Museum Timothy Ray Brown Women and HIV/AIDS Social AIDS orphan Catholic Church and HIV/AIDS Circumcision and HIV Criminal transmission Discrimination against people Economic impact Cost of treatment HIV-affected community HIV/AIDS activism HIV/AIDS denialism Red ribbon Safe sex Sex education List of HIV-positive people People With AIDS Self-Empowerment Movement HIV/AIDS in the porn industry Culture Discredited HIV/AIDS origins theories International AIDS Conference International AIDS Society Joint United Nations Programme on HIV/AIDS (UNAIDS) Media portrayal of HIV/AIDS Misconceptions about HIV/AIDS President's Emergency Plan for AIDS Relief (PEPFAR) The SING Campaign Solidays Treatment Action Campaign World AIDS Day YAA/Youthforce "Free Me" Larry Kramer Gay Men's Health Crisis ACT UP Silence=Death Project HIV/AIDS pandemic by region / country Africa Angola Benin Botswana Democratic Republic of the Congo Egypt Eswatini Ethiopia Ghana Guinea Côte d'Ivoire (Ivory Coast) Kenya Lesotho Madagascar Malawi Mali Mozambique Namibia Niger Nigeria Rwanda Senegal Tanzania South Africa Uganda Zambia Zimbabwe North America Canada Mexico El Salvador Guatemala Honduras Nicaragua United States New York City Caribbean Haiti Jamaica Dominican Republic South America Bolivia Brazil Colombia Guyana Peru Asia Afghanistan Armenia Azerbaijan Bahrain Bangladesh Bhutan Cambodia China (PRC) ( Yunnan ) East Timor India Indonesia Iran Iraq Japan Jordan North Korea Laos Malaysia Myanmar (Burma) Nepal Pakistan Philippines Saudi Arabia Sri Lanka Taiwan (ROC) Thailand United Arab Emirates Turkey Vietnam Europe United Kingdom Russia Ukraine Oceania Australia New Zealand Papua New Guinea List of countries by HIV/AIDS adult prevalence rate List of HIV/AIDS cases and deaths registered by region
  • Internet Addiction Disorder Wikipedia
    Signs and symptoms [ edit ] Physical symptoms [ edit ] Physical symptoms include a weakened immune system due to lack of sleep, loss of exercise, and increased the risk for carpel tunnel syndrome and eye and back strain. [11] Symptoms of withdrawal might include agitation, depression, anger and anxiety when the person is away from technology.
  • Leukoplakia Wikipedia
    It is one of the most common oral lesions associated with HIV infection, along with pseudomembraneous candidiasis. [12] The appearance of the lesion often heralds the transition from HIV to acquired immunodeficiency syndrome (AIDS). [12] Syphilitic leukoplakia [ edit ] This term refers to a white lesion associated with syphilis , specifically in the tertiary stage of the infection. [14] It is not considered to be a type of idiopathic leukoplakia, since the causative agent Treponema pallidum is known. ... External links [ edit ] Classification D ICD - 10 : K13.2 , N48.0 , N88.0 , N89.4 , N90.4 ICD - 9-CM : 528.6 , 530.83 , 607.0 , 622.2 , 623.1 , 624.0 MeSH : D007971 DiseasesDB : 7438 External resources MedlinePlus : 001046 Patient UK : Leukoplakia v t e Oral and maxillofacial pathology Lips Cheilitis Actinic Angular Plasma cell Cleft lip Congenital lip pit Eclabium Herpes labialis Macrocheilia Microcheilia Nasolabial cyst Sun poisoning Trumpeter's wart Tongue Ankyloglossia Black hairy tongue Caviar tongue Crenated tongue Cunnilingus tongue Fissured tongue Foliate papillitis Glossitis Geographic tongue Median rhomboid glossitis Transient lingual papillitis Glossoptosis Hypoglossia Lingual thyroid Macroglossia Microglossia Rhabdomyoma Palate Bednar's aphthae Cleft palate High-arched palate Palatal cysts of the newborn Inflammatory papillary hyperplasia Stomatitis nicotina Torus palatinus Oral mucosa – Lining of mouth Amalgam tattoo Angina bullosa haemorrhagica Behçet's disease Bohn's nodules Burning mouth syndrome Candidiasis Condyloma acuminatum Darier's disease Epulis fissuratum Erythema multiforme Erythroplakia Fibroma Giant-cell Focal epithelial hyperplasia Fordyce spots Hairy leukoplakia Hand, foot and mouth disease Hereditary benign intraepithelial dyskeratosis Herpangina Herpes zoster Intraoral dental sinus Leukoedema Leukoplakia Lichen planus Linea alba Lupus erythematosus Melanocytic nevus Melanocytic oral lesion Molluscum contagiosum Morsicatio buccarum Oral cancer Benign: Squamous cell papilloma Keratoacanthoma Malignant: Adenosquamous carcinoma Basaloid squamous carcinoma Mucosal melanoma Spindle cell carcinoma Squamous cell carcinoma Verrucous carcinoma Oral florid papillomatosis Oral melanosis Smoker's melanosis Pemphigoid Benign mucous membrane Pemphigus Plasmoacanthoma Stomatitis Aphthous Denture-related Herpetic Smokeless tobacco keratosis Submucous fibrosis Ulceration Riga–Fede disease Verruca vulgaris Verruciform xanthoma White sponge nevus Teeth ( pulp , dentin , enamel ) Amelogenesis imperfecta Ankylosis Anodontia Caries Early childhood caries Concrescence Failure of eruption of teeth Dens evaginatus Talon cusp Dentin dysplasia Dentin hypersensitivity Dentinogenesis imperfecta Dilaceration Discoloration Ectopic enamel Enamel hypocalcification Enamel hypoplasia Turner's hypoplasia Enamel pearl Fluorosis Fusion Gemination Hyperdontia Hypodontia Maxillary lateral incisor agenesis Impaction Wisdom tooth impaction Macrodontia Meth mouth Microdontia Odontogenic tumors Keratocystic odontogenic tumour Odontoma Dens in dente Open contact Premature eruption Neonatal teeth
    CTTN, TP53, MDM2, GSTT1, GSTM1, XRCC1, EGFR, BCL2, GSTM3, ERBB2, CYP1A1, DEFB4A, CDKN1A, CCND1, TGFB1, POLRMT, CIB2, PAX5, ABCB6, DLEC1, TP63, PABPN1, MFAP5, PRKDC, TFAM, PTGS2, RPE65, UVRAG, TP73, S100A4, PDPN, TLR4, TGM3, NAT1, RRAS2, CKAP4, POLG2, SIK1B, DEFB4B, MIR31, MIR29A, MIR21, GSTK1, LTO1, SIK1, SLCO6A1, DERL3, ARHGAP24, MTUS1, SLC12A9, EIF5A2, PIWIL2, TLR9, CD274, HPGDS, NOTCH1, NRAS, MMP13, NOS2, NELL2, FHIT, FGFR2, FGFR3, FGF2, ERCC2, ECT2, DNMT3B, DES, DEFB1, CYP2E1, COL4A1, CDKN2A, CDKN1C, CASP10, CASP7, CASP1, BSG, BRCA1, BAG1, GFAP, GSTP1, HOXC9, MCC, COX2, MSH2, MRE11, ATM, MMP9, MMP2, MLH1, MCL1, MAL, HOXC13, LCN2, LAMC2, KRT19, KRT13, KRT4, KRAS, IL10, IL6, MTCO2P12
    • Leukoplakia Mayo Clinic
      Overview With leukoplakia (loo-koh-PLAY-key-uh), thickened, white patches form on your gums, the insides of your cheeks, the bottom of your mouth and, sometimes, your tongue. These patches can't be scraped off. Doctors don't know what causes leukoplakia but consider chronic irritation from tobacco — whether smoked, dipped or chewed — to be the main culprit in its development. Most leukoplakia patches are noncancerous (benign), though some show early signs of cancer. Cancers on the bottom of the mouth can occur next to areas of leukoplakia. And white areas mixed in with red areas (speckled leukoplakia) may indicate the potential for cancer.
    • Leukoplakia GARD
      Leukoplakia is a condition in which thickened, white patches form on the tongue, gums, inside of the cheek, or sometimes on the outer female genitals. Although the sores can vary in appearance, they are usually white or gray; thick; and slightly raised with a hard surface. The condition is thought to be caused by irritation, but the cause is not always known. Tobacco is considered to be the main cause of its development in the mouth. Most patches are benign, but a small percentage show early signs of cancer.
  • Appendicitis Wikipedia
    Children: Gastroenteritis , mesenteric adenitis , Meckel's diverticulitis , intussusception , Henoch–Schönlein purpura , lobar pneumonia , urinary tract infection (abdominal pain in the absence of other symptoms can occur in children with UTI), new-onset Crohn's disease or ulcerative colitis , pancreatitis , and abdominal trauma from child abuse ; distal intestinal obstruction syndrome in children with cystic fibrosis; typhlitis in children with leukemia.
    CRP, ALB, SMUG1, SAA1, SAA2, SCN7A, CCL3, SELPLG, SOD1, TFE3, UCHL1, ADM, PTX3, NBAS, DEFB103B, ACSS2, HAMP, ACCS, LRG1, IS1, DEFB103A, PLA2G15, PITX2, PLAU, SERPINE1, AVP, RUNX3, DEFB1, DEFB4A, EDN1, HMGB1, IL3, IL5, IL6, IL6R, CXCL8, IL9, IL10, CXCL10, MYH9, NAGLU, NHS, DEFB4B
  • Haltlose Personality Disorder Wikipedia
    Personality disorder Haltlose personality disorder Other names - Willenlosen Psychopath [1] [2] [3] - Unstable psychopath [4] - Unstable drifter [5] [6] [7] - Disinhibited Personality [8] Specialty Psychiatry Usual onset Early adulthood [9] Duration Long term Causes - Maternal indolence (proposed) [10] - Childhood institutionalization (proposed) [10] - Parental rejection (proposed) [11] - Hereditary predisposition through the mother (proposed) [12] [13] Risk factors Parental neglect [10] Maternal alcoholism [14] Diagnostic method Based on reported symptoms Symptoms can be tested using TCI and ZKPQ [15] Differential diagnosis - ADHD [16] - Asthenic PD [17] - Delayed maturity [18] - Simplex or Disorganized schizophrenia [18] [19] - Epilepsy (When Haltlose is combined with alcoholism ) [20] [21] - Dependant PD [22] Prognosis - "Particularly unfavorable" regarding relapse [23] and long-term decline [24] - Can be controlled by external influence [25] [26] [18] - Although ideation and threats are common, typically lack the courage to commit suicide . [27] - Normal intelligence [28] Frequency Equal representation between males and females [13] Haltlose personality disorder is an ICD-10 personality disorder [29] in which affected individuals possess psychopathic traits built upon short-sighted selfishness [21] and irresponsible hedonism , combined with an inability to anchor one's identity to a future or past. [30] [31] The symptoms of Haltlose share similarities with frontal lobe syndrome , sociopathic and histrionic personality traits, [30] [32] and are characterized by a lack of inhibition [33] and "the immaturity of moral and volitional qualities...and the absence of positive ethical attitudes." [34] [ unreliable source?
  • Ego-Dystonic Sexual Orientation Wikipedia
    External links [ edit ] Classification D ICD - 10 : F66.1 v t e Mental and behavioral disorders Adult personality and behavior Gender dysphoria Ego-dystonic sexual orientation Paraphilia Fetishism Voyeurism Sexual maturation disorder Sexual relationship disorder Other Factitious disorder Munchausen syndrome Intermittent explosive disorder Dermatillomania Kleptomania Pyromania Trichotillomania Personality disorder Childhood and learning Emotional and behavioral ADHD Conduct disorder ODD Emotional and behavioral disorders Separation anxiety disorder Movement disorders Stereotypic Social functioning DAD RAD Selective mutism Speech Stuttering Cluttering Tic disorder Tourette syndrome Intellectual disability X-linked intellectual disability Lujan–Fryns syndrome Psychological development ( developmental disabilities ) Pervasive Specific Mood (affective) Bipolar Bipolar I Bipolar II Bipolar NOS Cyclothymia Depression Atypical depression Dysthymia Major depressive disorder Melancholic depression Seasonal affective disorder Mania Neurological and symptomatic Autism spectrum Autism Asperger syndrome High-functioning autism PDD-NOS Savant syndrome Dementia AIDS dementia complex Alzheimer's disease Creutzfeldt–Jakob disease Frontotemporal dementia Huntington's disease Mild cognitive impairment Parkinson's disease Pick's disease Sundowning Vascular dementia Wandering Other Delirium Organic brain syndrome Post-concussion syndrome Neurotic , stress -related and somatoform Adjustment Adjustment disorder with depressed mood Anxiety Phobia Agoraphobia Social anxiety Social phobia Anthropophobia Specific social phobia Specific phobia Claustrophobia Other Generalized anxiety disorder OCD Panic attack Panic disorder Stress Acute stress reaction PTSD Dissociative Depersonalization disorder Dissociative identity disorder Fugue state Psychogenic amnesia Somatic symptom Body dysmorphic disorder Conversion disorder Ganser syndrome Globus pharyngis Psychogenic non-epileptic seizures False pregnancy Hypochondriasis Mass psychogenic illness Nosophobia Psychogenic pain Somatization disorder Physiological and physical behavior Eating Anorexia nervosa Bulimia nervosa Rumination syndrome Other specified feeding or eating disorder Nonorganic sleep Hypersomnia Insomnia Parasomnia Night terror Nightmare REM sleep behavior disorder Postnatal Postpartum depression Postpartum psychosis Sexual dysfunction Arousal Erectile dysfunction Female sexual arousal disorder Desire Hypersexuality Hypoactive sexual desire disorder Orgasm Anorgasmia Delayed ejaculation Premature ejaculation Sexual anhedonia Pain Nonorganic dyspareunia Nonorganic vaginismus Psychoactive substances, substance abuse and substance-related Drug overdose Intoxication Physical dependence Rebound effect Stimulant psychosis Substance dependence Withdrawal Schizophrenia , schizotypal and delusional Delusional Delusional disorder Folie à deux Psychosis and schizophrenia-like Brief reactive psychosis Schizoaffective disorder Schizophreniform disorder Schizophrenia Childhood schizophrenia Disorganized (hebephrenic) schizophrenia Paranoid schizophrenia Pseudoneurotic schizophrenia Simple-type schizophrenia Other Catatonia Symptoms and uncategorized Impulse control disorder Klüver–Bucy syndrome Psychomotor agitation Stereotypy v t e Gender and sexual identities Gender identities Genders Man Woman Male Female Androgynos Androgyne Boi Cisgender Cross-dresser Gender bender Gender neutrality Non-binary (or genderqueer) Postgenderism Gender variance Transgender Trans man Trans woman Transsexual Third genders or third sexes Akava'ine Apwint Bakla Bugis genders Bissu Calabai Calalai Chibados Enaree Eunuch Fa'afafine Fakaleitī Femminiello Galli Hijra Kathoey Khanith Köçek Koekchuch Lhamana Māhū Mak nyah Mukhannathun Muxe Nádleehi Nullo Rae-rae Sipiniq Sworn virgin Takatāpui Travesti Tumtum Two-spirit Winkte Sexual orientation identities Sexual orientations Asexual Bisexual Heterosexual Homosexual Alternative labels Banjee Bi-curious Ex-gay Ex-ex-gay Gay Gray asexual Heteroflexible Lesbian Non-heterosexual Pansexual Polysexual Queer Questioning Same gender loving Social aspects Sociosexuality Antisexuality Monogamy Non-monogamy Polyamorous Asociality Homosociality Heterosociality Other Analloeroticism Androphilia and gynephilia Attraction to transgender people Kinsey scale Monosexuality Romantic orientation See also Gender roles Intersex Sex and gender distinction Sexuality and gender identity-based cultures Social construction of gender
  • Strabismus Wikipedia
    These letters of the alphabet denote ocular motility pattern that have a similarity to the respective letter: in the A-pattern there is (relatively speaking) more convergence when the gaze is directed upwards and more divergence when it is directed downwards, in the V-pattern it is the contrary, in the λ-, Y- and X-patterns there is little or no strabismus in the middle position but relatively more divergence in one or both of the upward and downward positions, depending on the "shape" of the letter. [40] Types of incomitant strabismus include: Duane syndrome , horizontal gaze palsy , and congenital fibrosis of the extraocular muscles . [41] When the misalignment of the eyes is large and obvious, the strabismus is called large-angle, referring to the angle of deviation between the lines of sight of the eyes. ... External links [ edit ] AAO Complex strabismus simulator UC Davis strabismus simulator Classification D ICD - 10 : H49 , H50 ICD - 9-CM : 378 OMIM : 185100 MeSH : D013285 DiseasesDB : 29577 External resources MedlinePlus : 001004 Patient UK : Strabismus v t e Diseases of the human eye Adnexa Eyelid Inflammation Stye Chalazion Blepharitis Entropion Ectropion Lagophthalmos Blepharochalasis Ptosis Blepharophimosis Xanthelasma Ankyloblepharon Eyelash Trichiasis Madarosis Lacrimal apparatus Dacryoadenitis Epiphora Dacryocystitis Xerophthalmia Orbit Exophthalmos Enophthalmos Orbital cellulitis Orbital lymphoma Periorbital cellulitis Conjunctiva Conjunctivitis allergic Pterygium Pseudopterygium Pinguecula Subconjunctival hemorrhage Globe Fibrous tunic Sclera Scleritis Episcleritis Cornea Keratitis herpetic acanthamoebic fungal Exposure Photokeratitis Corneal ulcer Thygeson's superficial punctate keratopathy Corneal dystrophy Fuchs' Meesmann Corneal ectasia Keratoconus Pellucid marginal degeneration Keratoglobus Terrien's marginal degeneration Post-LASIK ectasia Keratoconjunctivitis sicca Corneal opacity Corneal neovascularization Kayser–Fleischer ring Haab's striae Arcus senilis Band keratopathy Vascular tunic Iris Ciliary body Uveitis Intermediate uveitis Hyphema Rubeosis iridis Persistent pupillary membrane Iridodialysis Synechia Choroid Choroideremia Choroiditis Chorioretinitis Lens Cataract Congenital cataract Childhood cataract Aphakia Ectopia lentis Retina Retinitis Chorioretinitis Cytomegalovirus retinitis Retinal detachment Retinoschisis Ocular ischemic syndrome / Central retinal vein occlusion Central retinal artery occlusion Branch retinal artery occlusion Retinopathy diabetic hypertensive Purtscher's of prematurity Bietti's crystalline dystrophy Coats' disease Sickle cell Macular degeneration Retinitis pigmentosa Retinal haemorrhage Central serous retinopathy Macular edema Epiretinal membrane (Macular pucker) Vitelliform macular dystrophy Leber's congenital amaurosis Birdshot chorioretinopathy Other Glaucoma / Ocular hypertension / Primary juvenile glaucoma Floater Leber's hereditary optic neuropathy Red eye Globe rupture Keratomycosis Phthisis bulbi Persistent fetal vasculature / Persistent hyperplastic primary vitreous Persistent tunica vasculosa lentis Familial exudative vitreoretinopathy Pathways Optic nerve Optic disc Optic neuritis optic papillitis Papilledema Foster Kennedy syndrome Optic atrophy Optic disc drusen Optic neuropathy Ischemic anterior (AION) posterior (PION) Kjer's Leber's hereditary Toxic and nutritional Strabismus Extraocular muscles Binocular vision Accommodation Paralytic strabismus Ophthalmoparesis Chronic progressive external ophthalmoplegia Kearns–Sayre syndrome palsies Oculomotor (III) Fourth-nerve (IV) Sixth-nerve (VI) Other strabismus Esotropia / Exotropia Hypertropia Heterophoria Esophoria Exophoria Cyclotropia Brown's syndrome Duane syndrome Other binocular Conjugate gaze palsy Convergence insufficiency Internuclear ophthalmoplegia One and a half syndrome Refraction Refractive error Hyperopia Myopia Astigmatism Anisometropia / Aniseikonia Presbyopia Vision disorders Blindness Amblyopia Leber's congenital amaurosis Diplopia Scotoma Color blindness Achromatopsia Dichromacy Monochromacy Nyctalopia Oguchi disease Blindness / Vision loss / Visual impairment Anopsia Hemianopsia binasal bitemporal homonymous Quadrantanopia subjective Asthenopia Hemeralopia Photophobia Scintillating scotoma Pupil Anisocoria Argyll Robertson pupil Marcus Gunn pupil Adie syndrome Miosis Mydriasis Cycloplegia Parinaud's syndrome Other Nystagmus Childhood blindness Infections Trachoma Onchocerciasis Authority control GND : 4052363-9 NDL : 00571965
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SMC3, CTDP1, FIBP, AP4M1, ARHGEF2, SLC24A1, ZEB2, ARNT2, KIF14, CPLX1, FARS2, CLDN16, AP4B1, YME1L1, PLK4, RAI1, KDM5B, GJB6, SRCAP, MAFB, PNPLA6, CLP1, TLK2, MID2, AP4S1, LIPT1, PLPBP, HPS5, CTCF, MAB21L2, POMT1, DEAF1, AMMECR1, MED12, SLC12A6, DNM1L, HUWE1, PQBP1, LRPPRC, BCAP31, LPAR6, ALG3, CD96, APC2, YAP1, MAD2L2, PIBF1, COG5, SLC9A6, LARP7, BCL11A, PIGT, TMEM67, SLC9A7, WDR73, DISP1, PIGY, SHANK3, TUBGCP6, UBE3B, RSPRY1, RFT1, KRT74, NDUFAF2, STRADA, CACNA2D4, CEP41, KRT71, SCAMP4, CHST14, RAB39B, COL25A1, NKX6-2, SLX4, RNF135, FBXO11, ARMC9, NUBPL, WDR26, SLC19A3, COL18A1, ASXL3, SLC2A10, TRIM8, MED25, PUS3, MFRP, CDCA7, BRIP1, KIAA1109, ANTXR1, POMK, TWIST2, TRAPPC6B, CEP290, EOGT, HYLS1, JMJD1C, NALCN, CHAMP1, KANSL1, SLC13A5, LAMA1, UNC80, SLC6A19, MTFMT, LRIT3, TUBB2B, NDUFS7, NHLRC2, KIF7, ALG11, GPR179, PRSS56, ARL13B, LIPH, FCSK, UBR1, WDR81, NDUFA11, DMBX1, NAXE, PROKR2, EVC2, NDUFAF6, A2ML1, KRT25, B3GALNT2, CLDN19, SIK1, CEP120, VPS13B, ARX, ASXL1, ARID2, TTI2, L2HGDH, DYNC2LI1, ERMARD, OSGEP, PEX26, PACS1, FRMD4A, HHAT, NUP133, AGK, NGLY1, MCTP2, COQ8A, VPS11, CENPJ, TMEM126B, HDAC8, ZC4H2, NDUFA12, KLHL7, INPP5E, POMGNT1, FOXRED1, FANCI, SETD5, SUFU, ATP8A2, INPP5K, PEX11B, FGFRL1, PRMT7, TMCO1, NDUFB11, MAGEL2, DLL4, NSUN2, NCAPG2, MKS1, ADPRS, PHIP, FANCL, RFWD3, KIF15, CABP4, TCTN2, CCDC28B, NXN, SIL1, PORCN, TMEM237, RSRC2, CPLANE1, COLEC11, NDUFAF5, FA2H, GJC2, TMEM231, TCTN1, PALB2, SLC25A22, SNIP1, HPS6, EHMT1, CSPP1, NSD1, IFIH1, SLC39A8, PRDM16, SALL4, THOC2, MCOLN1, TBC1D24, SHROOM4, ARID1B, ARHGAP31, PCDH19, HACE1, CC2D2A, DOCK6, FANCM, MPP4, NYX, ALX4, TRAPPC11, PIEZO2, SUCLA2, DPM2, MPDZ, GNB1, GJA1, GK, GLI1, GLI2, GNAO1, GNAQ, GNAS, GNAT1, GNB3, HRAS, GP1BB, GRIA4, GRIN1, GRM6, GTF2I, H1-4, H3-3A, HNRNPU, GGCX, GFPT1, GBA, GATA4, FGF8, FGF14, FGFR1, FGFR3, FGFR2, FOXG1, FOXC1, FOXE3, FLI1, FLII, FLNA, FMR1, MTOR, FZD2, GABRD, GALC, GAS1, HOXA13, HSD17B4, NDUFS4, NDUFA4, ND3, TRIM37, MYH3, MYO5A, NAGA, NDP, NDUFA1, NDUFA2, NDUFA6, HSPD1, PTCH2, NDUFA10, NDUFB3, NDUFB9, NDUFB10, NDUFS1, NDUFS2, NDUFS3, ND2, ND1, KMT2A, MITF, HSPG2, IGF1R, RBPJ, KCNA1, KRAS, L1CAM, LAMB2, LBR, LETM1, LIG4, LIMK1, MAB21L1, SMAD4, MC1R, MDH2, MECP2, MEF2C, FGF3, FGD1, FKTN, CDH11, BRCA2, CA8, CACNA1A, CACNA1B, CAMK2A, CAMK2B, CDC42, CDH3, CHAT, FBN1, CHD3, LYST, CHRNA7, CHRNE, CHRNG, ERCC8, CLCN4, COL11A1, BRAF, BRCA1, FOXL2, BCS1L, ACOX1, ADSL, JAG1, AKT1, ALX3, SLC25A4, ARL3, ARVCF, ASCL1, ATM, RERE, ATP2B3, ALDH7A1, ATP6V1A, ATP6V1E1, ATR, BBS1, COL11A2, COMT, COX10, ELN, ERCC3, ERCC4, ERCC5, ERCC6, ERF, EVC, EXT2, EZH2, FANCA, FANCC, FANCD2, FANCE, ACSL4, BPTF, FANCB, FANCF, FANCG, ERCC2, EIF2S3, COX15, ECHS1, CRYAA, CTBP1, CYP1B1, DDB2, DDOST, DGUOK, DHCR7, DHCR24, DHODH, CYB5R3, DKC1, DLG3, SARDH, DMPK, DYNC1H1, DVL1, DVL3, NDUFV1, NDUFA9, NDUFS6, TCF20, VAMP1, SYT1, TAF1, MAP3K7, TBX1, TBX15, TCF4, TCF12, TCOF1, ABCC8, TDGF1, TFAP2A, TFAP2B, NR2F1, TGFBI, TGIF1, TRIO, HIRA, SURF1, STXBP1, SHH, SOS1, SIX3, SKI, SLC2A1, 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  • Mental Disorders And Gender Wikipedia
    Gay and bisexual men also experience a higher prevalence of full-syndrome bulimia and all subclinical eating disorders than their heterosexual counterparts. [58] Research has found lesbian women to have higher rates of weight-based self-worth and proneness to contracting eating disorders compared to gay men. [59] Lesbian women also experience comparable rates of eating disorders compared to heterosexual women, with similar rates of dieting , binge eating and purging behaviours. [59] However, lesbian women are more likely to report positive body image compared to heterosexual females (42.1% vs 20.5%). [59] Transgender individuals are significantly more likely than any other LGBTQ+ demographic to report an eating disorder diagnosis or compensatory behaviour related to eating. [60] Transgender individuals may use weight restriction to suppress secondary sex characteristics or to suppress or stress gendered features. [60] There is limited research regarding racial differences within LGBTQ+ populations as it relates to disordered eating. [61] Conflicting studies have struggled to ascertain whether LGBTQ+ people of colour experience similar or varying rates of eating disorder proneness or diagnosis. [61] Causes of gender disparities in mental disorders [ edit ] Violence against women [ edit ] There are different type of levels of violence that can occur against women. ... "Are eating disorders culture-bound syndromes? Implications for conceptualizing their etiology".
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