KEGG   DISEASE: 15q13.3 微細欠失症候群
エントリ  
H01877                                                             
名称    
15q13.3 微細欠失症候群
概要    
Chromosome 15q13.3 microdeletion syndrome causes a spectrum of cognitive disorders. The syndrome is caused by microdeletions in the 15q13.2q-13.3 region. This chromosomal region contains seven genes and is flanked by a breakpoint (BP) on each side. About 80% of patients with this syndrome have one or more neuropsychiatric diagnoses, including developmental disability/intellectual disability, autism spectrum disorder, speech problems, and attention deficit hyperactivity disorder (ADHD). The neuropsychiatric phenotypes of 15q13.3 microdeletion syndrome have been proposed to be caused by haploinsufficiency of CHRNA7, which is one of the seven genes.
カテゴリ  
染色体異常
階層分類  
ICD-11 による疾患分類 [BR:jp08403]
 20 発達異常
  遺伝子変異を除く染色体異常
   LD44  常染色体の欠失
    H01877  15q13.3 微細欠失症候群
病因遺伝子 
CHRNA7 [HSA:1139] [KO:K04809]
KLF13 [HSA:51621] [KO:K09208]
TRPM1 [HSA:4308] [KO:K04976]
FAN1 [HSA:22909] [KO:K15363]
コメント  
Other genes in the critical deleted region: MTMR10, MIR211, OTUD7A
リンク   
ICD-11: LD44.F
MeSH: C567439
OMIM: 612001
文献    
  著者
Crutcher E, Ali M, Harrison J, Sovago J, Gomez-Mancilla B, Schaaf CP
  タイトル
Assessment of Cognitive Outcome Measures in Teenagers with 15q13.3 Microdeletion Syndrome.
  雑誌
J Autism Dev Disord 46:1455-63 (2016)
DOI:10.1007/s10803-015-2694-0
文献    
  著者
Tropeano M, Andrieux J, Vassos E, Collier DA
  タイトル
Clinical utility gene card for: 15q13.3 microdeletion syndrome.
  雑誌
Eur J Hum Genet 22:ejhg201488 (2014)
DOI:10.1038/ejhg.2014.88
LinkDB    

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