KEGG   DISEASE: Bohring-Opitz 症候群
エントリ  
H02047                                                             
名称    
Bohring-Opitz 症候群
概要    
Bohring-Opitz syndrome (BOPS) is characterized by trigonocephaly and associated anomalies, such as unusual facies, psychomotor retardation, redundant skin, joint and limb abnormalities, and visceral anomalies. BOPS is considered the more severe form of the C syndrome [DS:H01008], therefore known as C-like syndrome. Recently, It has been reported that de novo nonsense mutations in ASXL1 cause BOPS.
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
   LD24  主な特徴として骨格の異常を伴う症候群
    H02047  Bohring-Opitz 症候群
パスウェイに基づく疾患分類 [BR:jp08402]
 細胞プロセス
  nt06523  ポリコーム複合体によるエピジェネティック制御
   H02047  Bohring-Opitz 症候群
ネットワーク
nt06523 Epigenetic regulation by Polycomb complexes
病因遺伝子 
ASXL1 [HSA:171023] [KO:K11471]
リンク   
ICD-11: LD24.GY
MeSH: C537419
OMIM: 605039
文献    
  著者
Bohring A, Oudesluijs GG, Grange DK, Zampino G, Thierry P
  タイトル
New cases of Bohring-Opitz syndrome, update, and critical review of the literature.
  雑誌
Am J Med Genet A 140:1257-63 (2006)
DOI:10.1002/ajmg.a.31265
文献    
  著者
Hoischen A, van Bon BW, Rodriguez-Santiago B, Gilissen C, Vissers LE, de Vries P, Janssen I, van Lier B, Hastings R, Smithson SF, Newbury-Ecob R, Kjaergaard S, Goodship J, McGowan R, Bartholdi D, Rauch A, Peippo M, Cobben JM, Wieczorek D, Gillessen-Kaesbach G, Veltman JA, Brunner HG, de Vries BB
  タイトル
De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome.
  雑誌
Nat Genet 43:729-31 (2011)
DOI:10.1038/ng.868
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