KEGG   DISEASE: 肩甲腓骨脊髄筋萎縮症
エントリ  
H00524                                                             
名称    
肩甲腓骨脊髄筋萎縮症
概要    
Scapuloperoneal spinal muscular atrophy (SPSMA) is one of the TRPV4-related diseases. They are a heterogeneous group of dominantly inherited disorders with muscle weakness. Mutations in TRPV4 have been linked to these disorders.
カテゴリ  
神経系疾患
階層分類  
ICD-11 による疾患分類 [BR:jp08403]
 08 神経系の疾患
  運動ニューロン疾患または関連症
   8B61  脊髄性筋萎縮症
    H00524  肩甲腓骨脊髄筋萎縮症
病因遺伝子 
TRPV4 [HSA:59341] [KO:K04973]
リンク   
ICD-11: 8B61.4
MeSH: D009134
OMIM: 181405
文献    
  著者
Dai J, Cho TJ, Unger S, Lausch E, Nishimura G, Kim OH, Superti-Furga A, Ikegawa S
  タイトル
TRPV4-pathy, a novel channelopathy affecting diverse systems.
  雑誌
J Hum Genet 55:400-2 (2010)
DOI:10.1038/jhg.2010.37
文献    
  著者
Fecto F, Shi Y, Huda R, Martina M, Siddique T, Deng HX
  タイトル
Mutant TRPV4-mediated toxicity is linked to increased constitutive function in axonal neuropathies.
  雑誌
J Biol Chem 286:17281-91 (2011)
DOI:10.1074/jbc.M111.237685
文献    
  著者
Zimon M, Baets J, Auer-Grumbach M, Berciano J, Garcia A, Lopez-Laso E, Merlini L, Hilton-Jones D, McEntagart M, Crosby AH, Barisic N, Boltshauser E, Shaw CE, Landoure G, Ludlow CL, Gaudet R, Houlden H, Reilly MM, Fischbeck KH, Sumner CJ, Timmerman V, Jordanova A, Jonghe PD
  タイトル
Dominant mutations in the cation channel gene transient receptor potential vanilloid 4 cause an unusual spectrum of neuropathies.
  雑誌
Brain 133:1798-809 (2010)
DOI:10.1093/brain/awq109
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