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  • Sulfonamide Hypersensitivity Syndrome Wikipedia
    External links [ edit ] Classification D ICD - 10 : Y40 ICD - 9-CM : E930.8 v t e Adverse drug reactions Antibiotics Penicillin drug reaction Sulfonamide hypersensitivity syndrome Urticarial erythema multiforme Adverse effects of fluoroquinolones Red man syndrome Jarisch–Herxheimer reaction Hormones Steroid acne Steroid folliculitis Chemotherapy Chemotherapy-induced acral erythema Chemotherapy-induced hyperpigmentation Scleroderma-like reaction to taxanes Hydroxyurea dermopathy Exudative hyponychial dermatitis Anticoagulants Anticoagulant-induced skin necrosis Warfarin necrosis Vitamin K reaction Texier's disease Immunologics Adverse reaction to biologic agents Leukotriene receptor antagonist-associated Churg–Strauss syndrome Methotrexate-induced papular eruption Adverse reaction to cytokines Other drugs Anticonvulsant hypersensitivity syndrome Allopurinol hypersensitivity syndrome Vaccine adverse event Eczema vaccinatum Bromoderma Halogenoderma Iododerma General Skin and body membranes Acute generalized exanthematous pustulosis Bullous drug reaction Drug-induced acne Drug-induced angioedema Drug-related gingival hyperplasia Drug-induced lichenoid reaction Drug-induced lupus erythematosus Drug-induced nail changes Drug-induced pigmentation Drug-induced urticaria Stevens–Johnson syndrome Injection site reaction Linear IgA bullous dermatosis Toxic epidermal necrolysis HIV disease-related drug reaction Photosensitive drug reaction Other Drug-induced pseudolymphoma Fixed drug reaction Serum sickness-like reaction This cutaneous condition article is a stub .
  • Methotrexate-Induced Papular Eruption Wikipedia
    You can help Wikipedia by expanding it . v t e v t e Adverse drug reactions Antibiotics Penicillin drug reaction Sulfonamide hypersensitivity syndrome Urticarial erythema multiforme Adverse effects of fluoroquinolones Red man syndrome Jarisch–Herxheimer reaction Hormones Steroid acne Steroid folliculitis Chemotherapy Chemotherapy-induced acral erythema Chemotherapy-induced hyperpigmentation Scleroderma-like reaction to taxanes Hydroxyurea dermopathy Exudative hyponychial dermatitis Anticoagulants Anticoagulant-induced skin necrosis Warfarin necrosis Vitamin K reaction Texier's disease Immunologics Adverse reaction to biologic agents Leukotriene receptor antagonist-associated Churg–Strauss syndrome Methotrexate-induced papular eruption Adverse reaction to cytokines Other drugs Anticonvulsant hypersensitivity syndrome Allopurinol hypersensitivity syndrome Vaccine adverse event Eczema vaccinatum Bromoderma Halogenoderma Iododerma General Skin and body membranes Acute generalized exanthematous pustulosis Bullous drug reaction Drug-induced acne Drug-induced angioedema Drug-related gingival hyperplasia Drug-induced lichenoid reaction Drug-induced lupus erythematosus Drug-induced nail changes Drug-induced pigmentation Drug-induced urticaria Stevens–Johnson syndrome Injection site reaction Linear IgA bullous dermatosis Toxic epidermal necrolysis HIV disease-related drug reaction Photosensitive drug reaction Other Drug-induced pseudolymphoma Fixed drug reaction Serum sickness-like reaction
  • Leukotriene Receptor Antagonist-Associated Churg–strauss Syndrome Wikipedia
    External links [ edit ] Classification D ICD - 10 : Y55.6 ICD - 9-CM : E945.7 v t e Adverse drug reactions Antibiotics Penicillin drug reaction Sulfonamide hypersensitivity syndrome Urticarial erythema multiforme Adverse effects of fluoroquinolones Red man syndrome Jarisch–Herxheimer reaction Hormones Steroid acne Steroid folliculitis Chemotherapy Chemotherapy-induced acral erythema Chemotherapy-induced hyperpigmentation Scleroderma-like reaction to taxanes Hydroxyurea dermopathy Exudative hyponychial dermatitis Anticoagulants Anticoagulant-induced skin necrosis Warfarin necrosis Vitamin K reaction Texier's disease Immunologics Adverse reaction to biologic agents Leukotriene receptor antagonist-associated Churg–Strauss syndrome Methotrexate-induced papular eruption Adverse reaction to cytokines Other drugs Anticonvulsant hypersensitivity syndrome Allopurinol hypersensitivity syndrome Vaccine adverse event Eczema vaccinatum Bromoderma Halogenoderma Iododerma General Skin and body membranes Acute generalized exanthematous pustulosis Bullous drug reaction Drug-induced acne Drug-induced angioedema Drug-related gingival hyperplasia Drug-induced lichenoid reaction Drug-induced lupus erythematosus Drug-induced nail changes Drug-induced pigmentation Drug-induced urticaria Stevens–Johnson syndrome Injection site reaction Linear IgA bullous dermatosis Toxic epidermal necrolysis HIV disease-related drug reaction Photosensitive drug reaction Other Drug-induced pseudolymphoma Fixed drug reaction Serum sickness-like reaction This cutaneous condition article is a stub .
  • Limbic-Predominant Age-Related Tdp-43 Encephalopathy Wikipedia
    The onset of LATE is generally thought to be slower than other types of dementia. [2] References [ edit ] ^ Nelson, Peter T; Dickson, Dennis W; Trojanowski, John T; Boyle, Patricia A; Arfanakis, Konstantinos; Rademakers, Rosa; Alafuzoff, Irina; Attems, Johannes; Brayne, Carol; Coyle-Gilchrist, Ian T S; Chui, Helena C; Fardo, David W; Flanagan, Margaret E; Halliday, Glenda; Hokkanen, Suvi R K; Hunter, Sally; Jicha, Gregory A; Katsumata, Yuriko; Kawas, Claudia H; Keene, C Dirk; Kovacs, Gabor G; Kukull, Walter A; Levey, Allan I; Makkinejad, Nazanin; Montine, Thomas J; Murayama, Shigeo; Murray, Melissa E; Nag, Sukriti; Rissman, Robert A; Seeley, William W; Sperling, Reisa A; White III, Charles L; Yu, Lei; Schneider, Julie A (30 April 2019).
  • Enostosis Wikipedia
    It is usually presented as a single lesion. [6] References [ edit ] ^ Ingle, John Ide; Bakland, Leif K. (2002). Endodontics . PMPH-USA. p. 197.
    SMUG1
  • Cystic Fibrosis–related Diabetes Wikipedia
    PMC 2992212 . PMID 21115770 . ^ Kayani K, Mohammed R, Mohiaddin H (2018-02-20).
  • Coprographia Wikipedia
    Cohen Georges Gilles de la Tourette Tim Howard Jean Marc Gaspard Itard Samuel Johnson James F. Leckman Arthur K. Shapiro Organizations Tourette Association of America Tourette Canada Tourettes Action Yale Child Study Center Media Front of the Class Hichki I Have Tourette's but Tourette's Doesn't Have Me John's Not Mad " Le Petit Tourette " Maze Motherless Brooklyn Quit It The Secret Life of Lele Pons The Tic Code Tic Talk: Living with Tourette Syndrome This article about a medical condition affecting the nervous system is a stub .
  • Antalgic Gait Wikipedia
    . ^ Walter, Kevin D. (2011). "Hip" Chapter 199. In Marcdante K, Kliegman R, Jenson H, Behrman R (Ed.), Nelson Essentials of Pediatrics (6th ed.) pp. 744-45.
  • Martorell's Ulcer Wikipedia
    . ^ Shutler, S. D.; Baragwanath, P.; Harding, K. G. (1995). "Martorell's ulcer" .
  • Folliculosebaceous Cystic Hamartoma Wikipedia
    PMID 18806500 . ^ Tanimura S, Arita K, Iwao F, et al. (January 2006). "Two cases of folliculosebaceous cystic hamartoma".
    ADGRV1
  • Ichthyosis With Confetti Wikipedia
    Cell . 148 (1–2): 33–45. doi : 10.1016/j.cell.2012.01.002 . PMID 22265400 . ^ Choate, K. A.; Lu, Y.; Zhou, J.; Choi, M.; Elias, P.
    KRT10, KRT1, TMEM99, KRT2
    • Ichthyosis With Confetti MedlinePlus
      Ichthyosis with confetti is a disorder of the skin. Individuals with this condition are born with red, scaly skin all over the body, which can be itchy in some people. In childhood or adolescence, hundreds to thousands of small patches of normal skin appear, usually on the torso. The numerous pale spots surrounded by red skin look like confetti, giving the condition its name. The patches of normal skin increase in number and size over time. In addition to red, scaly skin, people with ichthyosis with confetti typically have abnormally thick skin on the palms of the hands and soles of the feet (palmoplantar keratoderma). Many affected individuals have excess hair (hirsutism) on some parts of the body, particularly on the arms and legs.
    • Erythroderma, Ichthyosiform, Congenital Reticular OMIM
      A number sign (#) is used with this entry because of evidence that congenital reticular ichthyosiform erythroderma (CRIE) is caused by heterozygous mutation in the KRT10 gene (148080) on chromosome 17q21. Description Congenital reticular ichthyosiform erythroderma (CRIE), also known as ichthyosis with confetti (IWC), is a rare skin condition characterized by slowly enlarging islands of normal skin surrounded by erythematous ichthyotic patches in a reticulated pattern. The condition starts in infancy as a lamellar ichthyosis, with small islands of normal skin resembling confetti appearing in late childhood and at puberty. Histopathologic findings include band-like parakeratosis, psoriasiform acanthosis, and vacuolization of keratinocytes with binucleated cells in the upper epidermis, sometimes associated with amyloid deposition in the dermis. Ultrastructural abnormalities include perinuclear shells formed from a network of fine filaments in the upper epidermis (summary by Krunic et al., 2003).
  • Hyperostosis Wikipedia
    Hayem G, Bouchaud-Chabot A, Benali K, et al. (December 1999). "SAPHO syndrome: a long-term follow-up study of 120 cases".
    PTH, GALNT3, LEMD3, GNAQ, SLCO2A1, TGFB1, LRP5, WAS, WIPF1, PTEN, PSMB8, POLR3GL, SOST, FGFR3, FGF23, BMPR1A, SLC39A14, RPS19, CCL2, SPP1, TGFB2, TGFBI, TPH1, EBP, DLC1, ADAMTS1, OPLL, AKT1, PIK3CD, PIK3CG, GLI3, ANXA5, BGLAP, BMP2, RUNX2, DMP1, EXT1, EXT2, FLNA, HLA-B, ALPL, HTR1B, IGF1, LEP, LRP6, TNFRSF11B, PAPPA, PIK3CA, PIK3CB, AMER1
  • Androgen Deprivation-Induced Senescence Wikipedia
    References [ edit ] ^ Pernicová, Z; Slabáková, E; Kharaishvili, G; Bouchal, J; Král, M; Kunická, Z; Machala, M; Kozubík, A; Souček, K (June 2011). "Androgen depletion induces senescence in prostate cancer cells through down-regulation of Skp2" .
  • Cementoblastoma Wikipedia
    With incomplete removal, recurrence is common; some surgeons advocate curettage after extraction of teeth to decrease the overall rate of recurrence. [2] See also [ edit ] Cementum Cementogenesis Cementoblast References [ edit ] ^ Sankari Leena S, Ramakrishnan K (2011). "Benign cementoblastoma" .
    CD6, EZH2, MIR199A1, MIR199A2, MIR200C
    • Cementoma Wikipedia
      This article needs additional citations for verification . Please help improve this article by adding citations to reliable sources . Unsourced material may be challenged and removed. Find sources: "Cementoma" – news · newspapers · books · scholar · JSTOR ( October 2018 ) ( Learn how and when to remove this template message ) Cementoma Specialty Dentistry Human Tooth Diagram Cementoma is an odontogenic tumor of cementum . It is usually observed as a benign spherical mass of hard tissue fused to the root of a tooth. [1] It is found most commonly in the mandible in the region of the lower molar teeth , occurring between the ages of 8 to 30 in both sexes with equal frequency . [1] It causes distortion of surrounding areas but is usually a painless growth, at least initially. Considerable thickening of the cementum can often be observed. A periapical form is also recognized. Cementoma is not exclusive to the mandible as it can infrequently occur in the maxilla and other parts of the body such as the long bones. [2] Contents 1 Signs & Symptoms 1.1 Complications 2 Causes 3 Pathophysiology 4 Diagnosis 4.1 Differential diagnosis 5 Prevention/Treatment 6 Prognosis 7 Epidemiology 8 Research Directions 9 Types 10 See also 11 References 12 External links Signs & Symptoms [ edit ] Cementoma is characterized by a significant amount of thickening of the cementum around the roots of the teeth.
  • Fleischer Ring Wikipedia
    Münchener medizinische Wochenschrift . 53 : 625–626. ^ Hiratsuka Y, Nakayasu K, Kanai A (2000). "Secondary keratoconus with corneal epithelial iron ring similar to Fleischer's ring".
    ATP7B, CP
  • Verocay Body Wikipedia
    . ^ Pytel, Peter; Anthony, Douglas C. (2015). Kumar, Vinay; Abbas, Abul K.; Aster, Jon C. (eds.). Robbins and Cotran Pathologic Basis of Disease .
  • Squamous Metaplasia Wikipedia
    PMID 20155614 . ^ Kumar, Vinay; Abbas, Abul K.; Fausto, Nelson; & Mitchell, Richard N. (2007) Robbins Basic Pathology (8th ed.).
  • Rathke's Cleft Cyst Wikipedia
    Tom; Rebecca Chen; Sandeep Kunwar; Lewis Blevins; Manish K. Aghi (2015), "Incidence of headache as a presenting complaint in over 1,000 patients with sellar lesions and factors predicting postoperative improvement", Clinical Neurology and Neurosurgery , 132 (May 2015): 16–20, doi : 10.1016/j.clineuro.2015.02.006 , PMID 25746316 ^ Omar Islam (2008-05-28).
    BRAF, POMC, CTNNB1, LIF, EPCAM, NKX2-1, CLDN1
  • Oculofaciocardiodental Syndrome Wikipedia
    You can help by adding to it . ( December 2017 ) History [ edit ] The first features of this syndrome noted were the abnormal teeth, which were described by Hayward in 1980. [3] References [ edit ] ^ Surapornsawasd T, Ogawa T, Tsuji M, Moriyama K (June 2014). "Oculofaciocardiodental syndrome: novel BCOR mutations and expression in dental cells" .
    BCOR, GLI1, LAMB3, NFIC, NHS, OTC
    • Oculofaciocardiodental Syndrome Orphanet
      Oculo-facio-cardio-dental syndrome (OFCD) is a very rare multiple congenital anomaly syndrome characterized by dental radiculomegaly, congenital cataract, facial dismorphism and congenital heart disease. Epidemiology To date, 20 cases have been reported worldwide. Clinical description The most consistent and pathognomic dental finding of OFCD is radiculomegaly (extremely long roots), particularly of the canines and occasionally of other teeth including premolars and incisors. The dental eruption in both the deciduous and the permanent dentition is consistently slow and delayed. Oligodontia, fused teeth, supernumerary teeth, malformed permanent teeth, enamel defects, root dilacerations, malposition and malocclusion, have also been reported. Ocular abnormalities include bilateral congenital cataracts, microphthalmia, regressive vision impairment, secondary glaucoma, and ptosis.
    • Oculofaciocardiodental Syndrome GARD
      Oculofaciocardiodental syndrome is a genetic syndrome that affects the eyes, heart, face, and teeth. Common signs and symptoms include abnormally small deep-set eyes, cataracts, long narrow face, a broad nasal tip that is divided by a cleft, heart defects, and teeth with very large roots. Other signs and symptoms include glaucoma, cleft palate, delayed loss of baby teeth, missing or abnormally small teeth, misaligned teeth, and defective tooth enamel. Eye symptoms may involve one or both eyes.Oculofaciocardiodental syndrome is caused by mutations in the BCOR gene and is inherited in an X-linked dominant fashion .
    • Oculofaciocardiodental Syndrome MedlinePlus
      Oculofaciocardiodental (OFCD) syndrome is a condition that affects the development of the eyes (oculo-), facial features (facio-), heart (cardio-) and teeth (dental). This condition occurs only in females. The eye abnormalities associated with OFCD syndrome can affect one or both eyes . Many people with this condition are born with eyeballs that are abnormally small (microphthalmia). Other eye problems can include clouding of the lens (cataract ) and a higher risk of glaucoma , an eye disease that increases the pressure in the eye. These abnormalities can lead to vision loss or blindness. People with OFCD syndrome often have a long, narrow face with distinctive facial features, including deep-set eyes and a broad nasal tip that is divided by a cleft.
  • Lisch Epithelial Corneal Dystrophy Wikipedia
    . ^ Lisch W, Büttner A, Oeffner F, Böddeker I, Engel H, Lisch C, Ziegler A, Grzeschik K (October 2000). "Lisch corneal dystrophy is genetically distinct from Meesmann corneal dystrophy and maps to xp22.3".
    • Corneal Dystrophy, Lisch Epithelial OMIM
      Clinical Features Lisch et al. (1992) described 5 family members and 3 unrelated patients (4 males, 4 females), aged 23 to 71 years, with bilateral or unilateral, gray, band-shaped, and feathery opacities that sometimes appeared in whorled patterns. Retroillumination showed that the opacities consisted of intraepithelial, densely crowded, clear microcysts. Light and electron microscopy disclosed diffuse vacuolization of the cytoplasm of epithelial cells in the affected area. Visual acuity was so reduced in 3 patients that abrasion of the corneal epithelium was performed. The corneal abnormalities recurred within months, with the same reduction in visual acuity as before.
    • Lisch Epithelial Corneal Dystrophy Orphanet
      Lisch epithelial corneal dystrophy (LECD) is a very rare form of superficial corneal dystrophy characterized by feather-shaped opacities and microcysts in the corneal epithelium arranged in a band-shaped and sometimes whorled pattern, occasionally with impaired vision. Epidemiology Exact prevalence of this form of corneal dystrophy is not known but very few cases have been reported to date. LECD has been documented in one German family and in rare sporadic cases in Germany and the USA. Clinical description Lesions generally develop in childhood. Epithelial opacities are slowly progressive and painless blurred vision sometimes occurs after 60 years of age. Etiology The exact cause is unknown but appears to be genetic. The gene related to Lisch epithelial corneal dystrophy has been mapped to the short arm of the X chromosome (Xp22.3).
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