In this study, canakinumab was effective in patients with YAOS, and thus clinical trial of canakinumab may be warranted as a therapeutic option for this disease. [6] Inheritance [ edit ] Yao Syndrome inheritance is classified as Multifactorial Inheritance . [7] References [ edit ] ^ "Yao syndrome" . www.uniprot.org . ... The American Journal of Medicine . 130 (3): 365.e13–365.e18. doi : 10.1016/j.amjmed.2016.09.028 .

Idiopathic scrotal calcinosis Other names Idiopathic calcified nodules of the scrotum [1] Specialty Dermatology Idiopathic scrotal calcinosis is a cutaneous condition characterized by calcification of the skin resulting from the deposition of calcium and phosphorus occurring on the scrotum . [2] : 528 However, the levels of calcium and phosphate in the blood are normal. [3] Idiopathic scrotal calcinosis typically affects young males, with an onset between adolescence and early adulthood. [3] The scrotal calcinosis appears, without any symptoms, as yellowish nodules that range in size from 1 mm to several centimeters. [4] Contents 1 Presentation 2 Etiology 3 Diagnostic 4 Treatment 5 Prognosis 6 Epidemiology 7 History 8 See also 9 References Presentation [ edit ] Single or multiple hard, marble-like nodules of varying size affecting scrotal skin. ... "Scrotal Calcinosis". New England Journal of Medicine . 365 (7): 647. doi : 10.1056/NEJMicm1013803 . ... "Idiopathic scrotal calcinosis: a non-elucidated pathogenesis and its surgical treatment" . Reviews in Urology . 13 (2): 95–7. PMC 3176555 . PMID 21935341 . ^ Dubey S, Sharma R, Maheshwari V (2010).

The Psychiatric Quarterly . 26 (1): 365–371. doi : 10.1007/BF01568473 . PMID 14949213 . ^ Irena Milosevic; Randi E.

Contents 1 Signs and symptoms 2 Cause 3 Diagnosis 4 Treatment 5 History 6 References 7 External links Signs and symptoms [ edit ] TEMPI Symptom T Telangiectasias E Elevated Erythropoietin and Erythrocytosis M Monoclonal gammopathy P Perinephric fluid collections I Intrapulmonary shunting The patients were all diagnosed at middle age. ... "TEMPI Syndrome – A Novel Multisystem Disease" . N Engl J Med . 365 (5): 475–477. doi : 10.1056/NEJMc1106670 .

In the process of secretion, preprochymosin, comprising 381 amino acids, is processed by the signal peptidase into an inactive 365-amino acid prochymosin. At low pH, prochymosin undergoes autocatalytic cleavage of 42 N-terminal amino acids, yielding active chymosin.

It is a relatively uncommon variant of migraine in which the patient may experience aura , nausea , photophobia , hemiparesis , and other migraine symptoms , but does not experience headache . [1] It is generally classified as an event fulfilling the conditions of migraine with aura with no (or minimal) headache . [2] [3] It is sometimes distinguished from visual-only migraine aura without headache, also called ocular migraine . [4] Contents 1 Symptoms and misdiagnosis 2 Treatment 3 See also 4 References Symptoms and misdiagnosis [ edit ] Acephalgic migraines can occur in individuals of any age. [5] Some individuals, more commonly male, only experience acephalgic migraine, but frequently patients also experience migraine with headache. [6] Generally, the condition is more than twice as likely to occur in females than males. [7] Pediatric acephalgic migraines are listed along with other childhood periodic syndromes by W.A. ... Shevell as " migraine equivalents " (although not listed as such in the International Classification of Headache Disorders ), which can be good predictors of the future development of typical migraines. [8] [9] Individuals who experience acephalgic migraines in childhood are highly likely to develop typical migraines as they grow older. [10] Among women, incidents of acephalgic migraine increase during perimenopause . [7] Scintillating scotoma is the most common symptom [11] which usually happens concurrently with Expanding Fortification Spectra. [12] Also frequently reported is monocular blindness. [13] Acephalgic migraines typically do not persist more than a few hours and may last for as little as 15 seconds. [14] On rare occasions, they may continue for up to two days. [1] Acephalgic migraines may resemble transient ischemic attacks or, when longer in duration, stroke . [1] [15] The concurrence of other symptoms such as photophobia and nausea can help in determining the proper diagnosis. [15] Occasionally, patients with acephalgic migraine are misdiagnosed as suffering epilepsy with visual seizures , but the reverse misdiagnosis is more common. [16] Treatment [ edit ] The prevention and treatment of acephalgic migraine is broadly the same as for classical migraine , but the symptoms are usually less severe than those of classic migraine, so treatment is less likely to be required. ... "Pediatric migraine equivalents: occurrence and clinical features in practice". Pediatric Neurology . 26 (5): 365–8. doi : 10.1016/S0887-8994(01)00416-7 . ... McGraw-Hill Professional. p. 127. ISBN 0-07-105467-7 . ^ G. D. Schott (2007). "Exploring the visual hallucinations of migraine aura: the tacit contribution of illustration" . ... Clinical guide to comprehensive ophthalmology . Thieme. p. 532. ISBN 0-86577-766-7 . ^ Panayiotopoulos, Chrysostomos P. (2007).

"A homozygous mutation in LTBP2 causes isolated microspherophakia". Human Genetics . 128 (4): 365–371. doi : 10.1007/s00439-010-0858-8 .

. ^ Matsumoto T, Kuwabara N, Abe H, Fukuda Y, Suyama M, Fujii D, Kojima K, Futagawa S (1992), "Zahn infarct of the liver resulting from occlusive phlebitis in portal vein radicles", American Journal of Gastroenterology , 87 (3): 365–368, PMID 1539574 Reichelt HG (1985), "Partial Budd-Chiari syndrome with Zahn infarct of the liver in venous transmitted tumor thrombosis of a uterine cancer", Röntgen-Blätter (in German), 38 (11): 345–347, PMID 4081553 v t e Ischaemia and infarction Ischemia Location Brain ischemia Heart Large intestine Small intestine Infarction Types Anemic Hemorrhagic Location Heart Brain Spleen Limb Gangrene This article related to pathology is a stub .

ISBN 978-0-333-55313-8 . Retrieved 7 June 2018 . Comer, Ronald J. (2010). ... Archived from the original on 14 July 2017 . Retrieved 7 June 2018 . "FreeDictionary.com: definition of Hodophobia" . ... Archived from the original on 8 March 2012 . Retrieved 7 June 2018 . "CommonPhobias: Hodophobia" . Archived from the original on 2 October 2011 . Retrieved 7 June 2018 . "HealthCentral: Hodophobia" . ... Archived from the original on 2 October 2011 . Retrieved 7 June 2018 . * "Theravive: Specific Phobia DSM-5 300.29" .

., and Watanabe, T. 1966. " Phenazines as Disinfectants Against Bacterial Leaf Blight of the Rice Plant." Applied Microbiology 14(3):365-367. ^ Tisserat, N. "Ascochyta Leaf Blight of Turf" . ... Archived from the original on 30 October 2014. [1] [2] [3] [4] [5] [6] [7] [8] [9] [10] [11] [12] External links [ edit ] Media related to Blight at Wikimedia Commons The dictionary definition of blight at Wiktionary ^ Berg A. 1926. ... Canadian Journal of Microbiology; 19(7):837–845. ^ Johnson KB, Stockwell VO. 1998.

PMID 18252220 . https://web.archive.org/web/20060926021351/http://www.chromodisorder.org/sytrix/card_list.php3?dbid=63&id=365 An International System for Human Cytogenetic Nomenclature, Shaffer, L.G., Tommerup N. ... Karger, Basel 2005 v t e Chromosome abnormalities Autosomal Trisomies /Tetrasomies Down syndrome 21 Edwards syndrome 18 Patau syndrome 13 Trisomy 9 Tetrasomy 9p Warkany syndrome 2 8 Cat eye syndrome / Trisomy 22 22 Trisomy 16 Monosomies / deletions ( 1q21.1 copy number variations / 1q21.1 deletion syndrome / 1q21.1 duplication syndrome / TAR syndrome / 1p36 deletion syndrome ) 1 Wolf–Hirschhorn syndrome 4 Cri du chat syndrome / Chromosome 5q deletion syndrome 5 Williams syndrome 7 Jacobsen syndrome 11 Miller–Dieker syndrome / Smith–Magenis syndrome 17 DiGeorge syndrome 22 22q11.2 distal deletion syndrome 22 22q13 deletion syndrome 22 genomic imprinting Angelman syndrome / Prader–Willi syndrome ( 15 ) Distal 18q- / Proximal 18q- X / Y linked Monosomy Turner syndrome (45,X) Trisomy / tetrasomy , other karyotypes / mosaics Klinefelter syndrome (47,XXY) XXYY syndrome (48,XXYY) XXXY syndrome (48,XXXY) 49,XXXYY 49,XXXXY Triple X syndrome (47,XXX) Tetrasomy X (48,XXXX) 49,XXXXX Jacobs syndrome (47,XYY) 48,XYYY 49,XYYYY 45,X/46,XY 46,XX/46,XY Translocations Leukemia / lymphoma Lymphoid Burkitt's lymphoma t(8 MYC ;14 IGH ) Follicular lymphoma t(14 IGH ;18 BCL2 ) Mantle cell lymphoma / Multiple myeloma t(11 CCND1 :14 IGH ) Anaplastic large-cell lymphoma t(2 ALK ;5 NPM1 ) Acute lymphoblastic leukemia Myeloid Philadelphia chromosome t(9 ABL ; 22 BCR ) Acute myeloblastic leukemia with maturation t(8 RUNX1T1 ;21 RUNX1 ) Acute promyelocytic leukemia t(15 PML ,17 RARA ) Acute megakaryoblastic leukemia t(1 RBM15 ;22 MKL1 ) Other Ewing's sarcoma t(11 FLI1 ; 22 EWS ) Synovial sarcoma t(x SYT ;18 SSX ) Dermatofibrosarcoma protuberans t(17 COL1A1 ;22 PDGFB ) Myxoid liposarcoma t(12 DDIT3 ; 16 FUS ) Desmoplastic small-round-cell tumor t(11 WT1 ; 22 EWS ) Alveolar rhabdomyosarcoma t(2 PAX3 ; 13 FOXO1 ) t (1 PAX7 ; 13 FOXO1 ) Other Fragile X syndrome Uniparental disomy XX male syndrome / 46,XX testicular disorders of sex development Marker chromosome Ring chromosome 6 ; 9 ; 14 ; 15 ; 18 ; 20 ; 21 , 22

You can help by adding to it . ( September 2017 ) Treatment [ edit ] AON is a rare disease and the natural history of the disease process is not well defined. [7] Unlike typical optic neuritis, there is no association with multiple sclerosis, but the visual prognosis for AON is worse than typical optic neuritis. ... American Journal of Ophthalmology . 94 (1): 11–7. doi : 10.1016/0002-9394(82)90184-2 . ... "Systemic Lupus Erythematosus". New England Journal of Medicine . 365 (22): 2110–21. doi : 10.1056/NEJMra1100359 .

To investigate whether rs1617640 was specifically associated with diabetic microvascular complications rather than with complications of type 2 diabetes per se, the authors replicated the study in 365 patients with type 1 diabetes (222100) with both PDR and ESRD, 500 with nephropathy and retinopathy without progression to PDR and ESRD, and 574 type 1 diabetic control patients without nephropathy or retinopathy, and found that the T allele of rs1617640 was significantly associated (p = 2.66 x 10(-8)) with PDR and ESRD; the results were confirmed in a third cohort involving 379 type 1 diabetics with both PDR and nephropathy and 141 diabetic controls (p = 0.021).

Medical Examiner, Philadelphia, 1838, 1: 365–368. External links [ edit ] 01217 at CHORUS Classification D ICD - 10 : S52.5 External resources AO Foundation : – 21-C3 21-C1 – 21-C3 v t e Fractures and cartilage damage General Avulsion fracture Chalkstick fracture Greenstick fracture Open fracture Pathologic fracture Spiral fracture Head Basilar skull fracture Blowout fracture Mandibular fracture Nasal fracture Le Fort fracture of skull Zygomaticomaxillary complex fracture Zygoma fracture Spinal fracture Cervical fracture Jefferson fracture Hangman's fracture Flexion teardrop fracture Clay-shoveler fracture Burst fracture Compression fracture Chance fracture Holdsworth fracture Ribs Rib fracture Sternal fracture Shoulder fracture Clavicle Scapular Arm fracture Humerus fracture : Proximal Supracondylar Holstein–Lewis fracture Forearm fracture : Ulna fracture Monteggia fracture Hume fracture Radius fracture / Distal radius Galeazzi Colles' Smith's Barton's Essex-Lopresti fracture Hand fracture Scaphoid Rolando Bennett's Boxer's Busch's Pelvic fracture Duverney fracture Pipkin fracture Leg Tibia fracture : Bumper fracture Segond fracture Gosselin fracture Toddler's fracture Pilon fracture Plafond fracture Tillaux fracture Fibular fracture : Maisonneuve fracture Le Fort fracture of ankle Bosworth fracture Combined tibia and fibula fracture : Trimalleolar fracture Bimalleolar fracture Pott's fracture Crus fracture : Patella fracture Femoral fracture : Hip fracture Foot fracture Lisfranc Jones March Calcaneal This article about an injury is a stub .

In a 2-stage genomewide scan of 71 multicase leprosy families (365 individuals) in Brazil, Miller et al. (2004) found suggestive evidence for linkage to chromosomes 6p21.32, 17q22, and 20p13.

Mapping In a large 5-generation family (CM-13-OH) with CMAVM, Amyere et al. (2017) performed genomewide linkage analysis and detected 2 peaks with maximum lod scores of 2.5 and 2.8, on chromosomes 5 and 7, spanning 74.2 Mb and 59.1 Mb, respectively. Molecular Genetics In an 8-year-old white boy with multiple capillary malformations (CMs), who was negative for mutation in the RASA1 gene (139150), Yu et al. (2017) performed whole-exome sequencing (WES) and identified heterozygosity for a de novo missense mutation in the EPHB4 gene (D802G; 600011.0003). From a cohort of 365 index patients with CMAVM, Amyere et al. (2017) identified heterozygosity for 47 distinct mutations in the EPHB4 gene in 54 probands (see, e.g., 600011.0004-600011.0008).

. ^ "Dorlands Medical Dictionary:actinobacillosis" . [ permanent dead link ] ^ " Actinobacillosis - Pig reviewed and published by Wikivet" . Retrieved 7 October 2011 . ^ Layman, Quinci D.; Rezabek, Grant B.; Ramachandran, Akhilesh; Love, Brenda C.; Confer, Anthony W. (2014). ... Journal of Veterinary Diagnostic Investigation . 26 (3): 365–375. doi : 10.1177/1040638714531766 .

The condition appears to have been first described in the American medical literature by Samia Temtamy and John Rogers in 1976. [5] [6] Michael Cohen described it in 1979. [7] Only a few more than 200 cases have been confirmed worldwide, with estimates that about 120 people are currently alive with the condition. [8] As attenuated forms of the disease may exist, there could be many people with Proteus syndrome who remain undiagnosed. ... Contents 1 Signs and symptoms 1.1 Orthopaedic features 2 Genetics 3 Diagnosis 3.1 Differential diagnosis 3.2 Classification 4 Treatment 5 Notable cases 6 See also 7 References 8 External links Signs and symptoms [ edit ] Proteus syndrome causes an overgrowth of skin, bones, muscles, fatty tissues, and blood and lymphatic vessels. ... The New England Journal of Medicine . 365 (7): 661–3. doi : 10.1056/NEJMe1107384 . ... "A mosaic activating mutation in AKT1 associated with the Proteus syndrome" . N Engl J Med . 365 (7): 611–9. doi : 10.1056/NEJMoa1104017 . ... Am. J. Med. Genet. A . 130A (2): 123–7. doi : 10.1002/ajmg.a.30335 . PMID 15372512 .

"Identification of two mutations in human xanthine dehydrogenase gene responsible for classical type I xanthinuria" . J. Clin. Invest. 99 (10): 2391–7. doi : 10.1172/JCI119421 . PMC 508078 . ... "Identification of two mutations in human xanthine dehydrogenase gene responsible for classical type I xanthinuria" . J Clin Invest . 99 (10): 2391–7. doi : 10.1172/JCI119421 . PMC 508078 . ... Clin Chim Acta . 137 (2): 189–98. doi : 10.1016/0009-8981(84)90179-7 . PMID 6423323 . Hille R. (2006). ... External links [ edit ] Classification D ICD - 10 : E79.8 ICD - 9-CM : 277.2 OMIM : 278300 603592 MeSH : C566358, C566358, C562584 C562584, C566358, C566358, C562584 DiseasesDB : 14194 SNOMED CT : 190919008 External resources eMedicine : ped/2452 Xanthinuria at NIH 's Office of Rare Diseases v t e Inborn error of purine–pyrimidine metabolism Purine metabolism Anabolism Adenylosuccinate lyase deficiency Adenosine Monophosphate Deaminase Deficiency type 1 Nucleotide salvage Lesch–Nyhan syndrome / Hyperuricemia Adenine phosphoribosyltransferase deficiency Catabolism Adenosine deaminase deficiency Purine nucleoside phosphorylase deficiency Xanthinuria Gout Mitochondrial neurogastrointestinal encephalopathy syndrome Pyrimidine metabolism Anabolism Orotic aciduria Miller syndrome Catabolism Dihydropyrimidine dehydrogenase deficiency v t e Purine receptor modulators Receptor ( ligands ) P0 ( adenine ) Agonists: 8-Aminoadenine Adenine P1 ( adenosine ) Agonists: 2-(1-Hexynyl)- N -methyladenosine 2-Cl-IB-MECA 2'-MeCCPA 4'-O-β-D-Glucosyl-9-O-(6''-deoxysaccharosyl)olivil 5'- N -ethylcarboxamidoadenosine Adenosine ADP AMP Apadenoson ATL-146e ATP BAY 60–6583 Binodenoson Capadenoson CCPA CGS-21680 CP-532,903 Evodenoson GR 79236 LUF-5835 LUF-5845 N 6 -Cyclopentyladenosine Namodenoson Neladenoson dalanate Piclidenoson Regadenoson SDZ WAG 994 Selodenoson Sonedenoson Tecadenoson UK-432,097 Antagonists: 8-Chlorotheophylline 8-Phenyl-1,3-dipropylxanthine 8-Phenyltheophylline Acefylline Aminophylline ATL-444 Bamifylline Cafedrine Caffeine Caffeine citrate Cartazolate CGH-2466 CGS-15943 Choline theophyllinate Ciforadenant CPX CVT-6883 Dimethazan DMPX DPCPX Dyphylline Enprofylline Etazolate Fenethylline IBMX Isovaleric acid Istradefylline KF-26777 MRE3008F20 MRS-1220 MRS-1334 MRS-1706 MRS-1754 MRS-3777 Paraxanthine Pentoxifylline Preladenant Propentofylline Proxyphylline PSB-10 PSB-11 PSB-36 PSB-603 PSB-788 PSB-1115 Reversine Rolofylline SCH-442,416 SCH-58261 Theacrine Theobromine Theodrenaline Theophylline Tozadenant Tracazolate VUF-5574 ZM-241,385 P2 ( nucleotide ) P2X ( ATP ) Agonists: 2-Me-SATP α,β-Me-ATP Adenosine ADP AMP Ap4A Ap5A ATP ATPγS BzATP Cibacron blue CTP D-β,γ-Me-ATP GTP HT-AMP Ivermectin L-β,γ-Me-ATP MRS-2219 PAPET-ATP UTP Zinc Antagonists: 5-BDBD A-317491 A-438079 A-740003 A-804598 A-839977 AF-353 AZ-10606120 AZ-11645373 BBG Calcium Calmidazolium Chelerythrine Copper Emodin ( Rheum officinale ) Evans Blue Gefapixant GW-791343 HMA Ip5I isoPPADS JNJ-47965567 KN-04 KN-62 Magnesium MRS-2159 NF-023 NF-110 NF-157 NF-279 NF-449 Opiranserin (VVZ-149) Oxidized-ATP Phenol Red Phenolphthalein PPADS PPNDS PSB-12062 Puerarin ( Radix puerariae ) Purotoxin 1 RB-2 Ro 0437626 Ro 51 RO-3 Sodium ferulate ( Angelica sinensis , Ligusticum wallichii ) Suramin TC-P 262 Tetramethylpyrazine (ligustrazine) ( Ligusticum wallichii ) TNP-ATP Zinc P2Y Agonists: 2-Me-SADP 2-Me-SATP 2-Thio-UTP 5-Br-UDP 5-OMe-UDP α,β-Me-ATP Adenosine ADP ADPβS Ap3A AR-C 67085MX ATP ATPγS CTP dATP Denufosol Diquafosol IDP ITP INS-365 INS-37217 MRS-2365 MRS-2690 MRS-2693 MRS-2768 MRS-2957 MRS-4062 NF-546 PAPET-ATP PSB-0474 PSB-1114 UDP UDPβS UDP-galactose UDP-glucose UDP-N-acetylglucosamine Up3U UTP UTPγS Antagonists: 2-Me-SAMP A3P5PS AMPαS Ap4A AR-C 66096 AR-C 67085MX AR-C 69931MX AR-C 118925XX ATP BzATP C1330-7 Cangrelor Clopidogrel Elinogrel Ip5I MRS-2179 MRS-2211 MRS-2279 MRS-2395 MRS-2500 MRS-2578 NF-157 NF-340 PIT PPADS Prasugrel PSB-0739 RB-2 Regrelor Suramin Ticagrelor Ticlopidine UDP Transporter ( blockers ) CNTs 6-Hydroxy-7-methoxyflavone Adenosine dMeThPmR Estradiol KGO-2142 KGO-2173 MeThPmR Phloridzin Progesterone ENTs Barbiturates Benzodiazepines Cilostazol Dilazep Dipyridamole Estradiol Ethanol Hexobendine NBMPR Pentoxifylline Progesterone Propentofylline PMAT Decynium-22 Enzyme ( inhibitors ) XO Allopurinol Amflutizole Benzbromarone Caffeic acid Cinnamaldehyde Cinnamomum osmophloeum Febuxostat Myo-inositol Kaempferol Myricetin Niraxostat Oxipurinol Phytic acid Pistacia integerrima Propolis Quercetin Tisopurine Topiroxostat Others Aminopterin Azathioprine Methotrexate Mycophenolic acid Pemetrexed Pralatrexate Many others Others Precursors: Adenine Adenosine AMP ADP ATP Cytosine Cytidine CMP CDP CTP Guanine Guanosine GMP GDP GTP Hypoxanthine Inosine IMP IDP ITP Ribose Uracil Uridine UMP UDP UTP Others: Chrysophanol ( rhubarb ) See also: Receptor/signaling modulators

"Prognostic value of Y deletion analysis" . Human Reproduction . 15 (7): 1431–1434. doi : 10.1093/humrep/15.7.1431 . ... "Screening for Y chromosome microdeletions in idiopathic and nonidiopathic infertile men with varicocele and cryptorchidism" . Chin. Med. J . 118 (17): 1462–7. PMID 16157049 . ^ Poongothai J, Gopenath TS, Manonayaki S (April 2009). ... Acta Med Port (in Portuguese). 11 (4): 365–72. PMID 9644848 . Further reading [ edit ] GeneReviews/NCBI/NIH/UW entry on Y Chromosome Infertility v t e Chromosome abnormalities Autosomal Trisomies /Tetrasomies Down syndrome 21 Edwards syndrome 18 Patau syndrome 13 Trisomy 9 Tetrasomy 9p Warkany syndrome 2 8 Cat eye syndrome / Trisomy 22 22 Trisomy 16 Monosomies / deletions ( 1q21.1 copy number variations / 1q21.1 deletion syndrome / 1q21.1 duplication syndrome / TAR syndrome / 1p36 deletion syndrome ) 1 Wolf–Hirschhorn syndrome 4 Cri du chat syndrome / Chromosome 5q deletion syndrome 5 Williams syndrome 7 Jacobsen syndrome 11 Miller–Dieker syndrome / Smith–Magenis syndrome 17 DiGeorge syndrome 22 22q11.2 distal deletion syndrome 22 22q13 deletion syndrome 22 genomic imprinting Angelman syndrome / Prader–Willi syndrome ( 15 ) Distal 18q- / Proximal 18q- X / Y linked Monosomy Turner syndrome (45,X) Trisomy / tetrasomy , other karyotypes / mosaics Klinefelter syndrome (47,XXY) XXYY syndrome (48,XXYY) XXXY syndrome (48,XXXY) 49,XXXYY 49,XXXXY Triple X syndrome (47,XXX) Tetrasomy X (48,XXXX) 49,XXXXX Jacobs syndrome (47,XYY) 48,XYYY 49,XYYYY 45,X/46,XY 46,XX/46,XY Translocations Leukemia / lymphoma Lymphoid Burkitt's lymphoma t(8 MYC ;14 IGH ) Follicular lymphoma t(14 IGH ;18 BCL2 ) Mantle cell lymphoma / Multiple myeloma t(11 CCND1 :14 IGH ) Anaplastic large-cell lymphoma t(2 ALK ;5 NPM1 ) Acute lymphoblastic leukemia Myeloid Philadelphia chromosome t(9 ABL ; 22 BCR ) Acute myeloblastic leukemia with maturation t(8 RUNX1T1 ;21 RUNX1 ) Acute promyelocytic leukemia t(15 PML ,17 RARA ) Acute megakaryoblastic leukemia t(1 RBM15 ;22 MKL1 ) Other Ewing's sarcoma t(11 FLI1 ; 22 EWS ) Synovial sarcoma t(x SYT ;18 SSX ) Dermatofibrosarcoma protuberans t(17 COL1A1 ;22 PDGFB ) Myxoid liposarcoma t(12 DDIT3 ; 16 FUS ) Desmoplastic small-round-cell tumor t(11 WT1 ; 22 EWS ) Alveolar rhabdomyosarcoma t(2 PAX3 ; 13 FOXO1 ) t (1 PAX7 ; 13 FOXO1 ) Other Fragile X syndrome Uniparental disomy XX male syndrome / 46,XX testicular disorders of sex development Marker chromosome Ring chromosome 6 ; 9 ; 14 ; 15 ; 18 ; 20 ; 21 , 22