KEGG   DISEASE: 全般的発達遅滞・脳梁形成不全および顔異形症
エントリ  
H02376                                                             
名称    
全般的発達遅滞・脳梁形成不全および顔異形症
概要    
Global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies (GDACCF) is a syndromic intellectual disability with corpus callosum anomalies and short stature as shared features. It may be accompanied by microcephaly, feeding problems, and variable facial features. Truncating de novo mutations in the Kruppel-type zinc-finger gene ZNF148 have been reported in patients.
カテゴリ  
先天奇形
階層分類  
ICD-11 による疾患分類 [BR:jp08403]
 20 発達異常
  多発性の発達異常または症候群
   LD2F  多発性の構造異常を伴う症候群, 主な体系の関与を伴わないもの
    H02376  全般的発達遅滞・脳梁形成不全および顔異形症
病因遺伝子 
ZNF148 [HSA:7707] [KO:K24370]
リンク   
ICD-11: LD2F.1Y
OMIM: 617250
文献    
  著者
Stevens SJ, van Essen AJ, van Ravenswaaij CM, Elias AF, Haven JA, Lelieveld SH, Pfundt R, Nillesen WM, Yntema HG, van Roozendaal K, Stegmann AP, Gilissen C, Brunner HG
  タイトル
Truncating de novo mutations in the Kruppel-type zinc-finger gene ZNF148 in patients with corpus callosum defects, developmental delay, short stature, and dysmorphisms.
  雑誌
Genome Med 8:131 (2016)
DOI:10.1186/s13073-016-0386-9
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