KEGG   DISEASE: Laing 遠位型ミオパチー
エントリ  
H01977                                                             
名称    
Laing 遠位型ミオパチー;
遠位型ミオパチー 1
  上位グループ
遠位型ミオパチー [DS:H00594]
概要    
Laing distal myopathy (MPD1) is an early onset autosomal dominant distal myopathy. Selective weakness of the anterior tibial muscles is followed by weakness of the finger extensors and of selected proximal muscle groups, such as the abductors and rotators. This disease is caused by mutations in MYH7, the gene encoding the myosin heavy chain, which is expressed in type 1 fibers of skeletal muscle and in the heart.
カテゴリ  
神経系疾患; 筋骨格疾患
階層分類  
ICD-11 による疾患分類 [BR:jp08403]
 08 神経系の疾患
  神経筋接合部または筋の疾患
   原発性筋疾患
    8C75  遠位型ミオパチー
     H01977  Laing 遠位型ミオパチー
病因遺伝子 
MYH7 [HSA:4625] [KO:K17751]
リンク   
ICD-11: 8C75
MeSH: D049310
OMIM: 160500
文献    
  著者
Darin N, Tajsharghi H, Ostman-Smith I, Gilljam T, Oldfors A
  タイトル
New skeletal myopathy and cardiomyopathy associated with a missense mutation in MYH7.
  雑誌
Neurology 68:2041-2 (2007)
DOI:10.1212/01.wnl.0000264430.55233.72
文献    
  著者
Meredith C, Herrmann R, Parry C, Liyanage K, Dye DE, Durling HJ, Duff RM, Beckman K, de Visser M, van der Graaff MM, Hedera P, Fink JK, Petty EM, Lamont P, Fabian V, Bridges L, Voit T, Mastaglia FL, Laing NG
  タイトル
Mutations in the slow skeletal muscle fiber myosin heavy chain gene (MYH7) cause laing early-onset distal myopathy (MPD1).
  雑誌
Am J Hum Genet 75:703-8 (2004)
DOI:10.1086/424760
LinkDB    

» English version

DBGET integrated database retrieval system