KEGG   DISEASE: 家族性心室頻拍
エントリ  
H02269                                                             
名称    
家族性心室頻拍
概要    
Sudden cardiac death resulting from ventricular tachyarrhythmia represents a major healthcare issue. Familial ventricular tachycardia is usually attributable to recognized conditions such as arrhythmogenic right ventricular dysplasia, hypertrophic cardiomyopathy, familial cardiomyopathy or one of the long QT interval syndromes. However, some patients had no specific electrocardiographic (ECG) changes. Their QT intervals were normal and showed no cardiac abnormalities. It has been reported that absence of the inhibitory G-Protein (G alpha i-2) predisposes to ventricular tachycardia.
カテゴリ  
循環器系疾患
階層分類  
ICD-11 による疾患分類 [BR:jp08403]
 11 循環器系の疾患
  不整脈
   心室調律異常
    BC71  心室頻脈性不整脈
     H02269  家族性心室頻拍
病因遺伝子 
GNAI2 [HSA:2771] [KO:K04630]
リンク   
ICD-11: BC71.0Y
MeSH: D017180
OMIM: 192605
文献    
  著者
Fisher JD, Krikler D, Hallidie-Smith KA
  タイトル
Familial polymorphic ventricular arrhythmias: a quarter century of successful medical treatment based on serial exercise-pharmacologic testing.
  雑誌
J Am Coll Cardiol 34:2015-22 (1999)
DOI:10.1016/S0735-1097(99)00438-6
文献    
  著者
Zuberi Z, Nobles M, Sebastian S, Dyson A, Lim SY, Breckenridge R, Birnbaumer L, Tinker A
  タイトル
Absence of the inhibitory G-protein Galphai2 predisposes to ventricular cardiac arrhythmia.
  雑誌
Circ Arrhythm Electrophysiol 3:391-400 (2010)
DOI:10.1161/CIRCEP.109.894329
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