KEGG   DISEASE: 常同性運動・てんかん および/または大脳奇形を伴う精神遅滞
エントリ  
H01223                      Disease                                
名称    
常同性運動・てんかん および/または大脳奇形を伴う精神遅滞;
5q14.3 欠失症候群
概要    
Mental retardation-stereotypic movements-epilepsy and/or cerebral malformations (MRSME) is a disorder characterized by severe mental retardation, absent speech, hypotonia, poor eye contact and stereotypic movements. Most of the patients presented also with facial dysmorphic features, epilepsy and cerebral malformations. It has been suggested that haploinsufficiency of MEF2C is responsible for MRSME.
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
    H01223  常同性運動・てんかん および/または大脳奇形を伴う精神遅滞
病因遺伝子 
MEF2C [HSA:4208] [KO:K04454]
リンク   
ICD-11: LD44.50
OMIM: 613443
文献    
  著者
Le Meur N, Holder-Espinasse M, Jaillard S, Goldenberg A, Joriot S, Amati-Bonneau P, Guichet A, Barth M, Charollais A, Journel H, Auvin S, Boucher C, Kerckaert JP, David V, Manouvrier-Hanu S, Saugier-Veber P, Frebourg T, Dubourg C, Andrieux J, Bonneau D
  タイトル
MEF2C haploinsufficiency caused by either microdeletion of the 5q14.3 region or mutation is responsible for severe mental retardation with stereotypic movements, epilepsy and/or cerebral malformations.
  雑誌
J Med Genet 47:22-9 (2010)
DOI:10.1136/jmg.2009.069732
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