KEGG   DISEASE: Borjeson-Forssman-Lehmann 症候群
エントリ  
H01915                                                             
名称    
Borjeson-Forssman-Lehmann 症候群
  上位グループ
X 連鎖知的発達障害症候群 [DS:H00658]
概要    
Borjeson-Forssman-Lehmann syndrome (BFLS) is a rare, X-linked mental retardation syndrome. BFLS is characterized by severe intellectual disability, epilepsy, microcephaly, coarse facial features, long ears, short stature, obesity, gynecomastia, tapering fingers, and shortened toes. Mutations in the zinc finger gene PHF6 are the cause of BFLS.
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
   LD29  主な特徴として肥満を伴う症候群
    H01915  Borjeson-Forssman-Lehmann 症候群
病因遺伝子 
PHF6 [HSA:84295] [KO:K23310]
コメント  
See also H00658 Syndromic X-linked mental retardation.
リンク   
ICD-11: LD29
MeSH: C536575
OMIM: 301900
文献    
  著者
Gecz J, Turner G, Nelson J, Partington M
  タイトル
The Borjeson-Forssman-Lehman syndrome (BFLS, MIM #301900).
  雑誌
Eur J Hum Genet 14:1233-7 (2006)
DOI:10.1038/sj.ejhg.5201639
文献    
  著者
Turner G, Lower KM, White SM, Delatycki M, Lampe AK, Wright M, Smith JC, Kerr B, Schelley S, Hoyme HE, De Vries BB, Kleefstra T, Grompe M, Cox B, Gecz J, Partington M
  タイトル
The clinical picture of the Borjeson-Forssman-Lehmann syndrome in males and heterozygous females with PHF6 mutations.
  雑誌
Clin Genet 65:226-32 (2004)
DOI:10.1111/j.0009-9163.2004.00215.x
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