KEGG   DISEASE: 先天性拘縮性クモ指症
エントリ  
H00660                                                             
名称    
先天性拘縮性クモ指症;
Beals 症候群
  上位グループ
遠位関節拘縮症 [DS:H00811]
概要    
Congenital contractural arachnodactyly (CCA) or Beals syndrome is an autosomal dominant disorder characterized by a Marfan-like appearance and arachnodactyly. Most affected individuals have 'crumpled' ears, contractures of major joints, and camptodactyly. Additional features include muscular hypoplasia and scoliosis. In contrast to Marfan syndrome, CCA does not affect the aorta or the eyes.
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
   LD28  主な特徴として結合組織の異常を伴う症候群
    H00660  先天性拘縮性クモ指症
病因遺伝子 
FBN2 [HSA:2201] [KO:K23342]
コメント  
For Marfan syndrome, see H00653.
リンク   
ICD-11: LD28.00
MeSH: C536211
OMIM: 121050
文献    
  著者
Robinson PN, Arteaga-Solis E, Baldock C, Collod-Beroud G, Booms P, De Paepe A, Dietz HC, Guo G, Handford PA, Judge DP, Kielty CM, Loeys B, Milewicz DM, Ney A, Ramirez F, Reinhardt DP, Tiedemann K, Whiteman P, Godfrey M
  タイトル
The molecular genetics of Marfan syndrome and related disorders.
  雑誌
J Med Genet 43:769-87 (2006)
DOI:10.1136/jmg.2005.039669
文献    
  著者
Robinson PN, Godfrey M
  タイトル
The molecular genetics of Marfan syndrome and related microfibrillopathies.
  雑誌
J Med Genet 37:9-25 (2000)
DOI:10.1136/jmg.37.1.9
文献    
PMID:7493032
  著者
Putnam EA, Zhang H, Ramirez F, Milewicz DM
  タイトル
Fibrillin-2 (FBN2) mutations result in the Marfan-like disorder, congenital contractural arachnodactyly.
  雑誌
Nat Genet 11:456-8 (1995)
DOI:10.1038/ng1295-456
文献    
  著者
Godfrey M
  タイトル
Congenital Contractural Arachnodactyly
  雑誌
GeneReviews (1993)
LinkDB    

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