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Results 1 - 10 of 10 for Brugada syndrome 6
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  1. KCNH2 gene 
    ... Guerchicoff A, Bianchi F, Giustetto C, Schimpf R, Brugada P, Antzelevitch C. Sudden death associated with short-QT syndrome linked to mutations in HERG. Circulation. 2004 Jan 6;109(1):30-5. doi: 10.1161/01. ...
    https://medlineplus.gov/genetics/gene/kcnh2 - Genetics
  2. Progressive familial heart block 
    ... CR. Sodium channel beta1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans. J Clin Invest. 2008 Jun;118(6):2260-8. doi: 10.1172/JCI33891. Citation on ...
    https://medlineplus.gov/.../progressive-familial-heart-block - Genetics
  3. Brugada syndrome 
    ... 1.2.177. Citation on PubMed Brugada P, Brugada J. Right bundle branch block, persistent ST segment elevation and sudden cardiac death: a distinct clinical and electrocardiographic syndrome. A multicenter report. J Am Coll Cardiol. 1992 Nov 15;20(6):1391-6. doi: 10.1016/0735-1097(92) ...
    https://medlineplus.gov/genetics/condition/brugada-syndrome - Genetics
  4. SCN5A gene 
    ... SCN5A gene have been identified in people with Brugada syndrome, which is a heart condition characterized by an ... populations. Researchers have since determined that SUNDS and Brugada syndrome are the same disorder.Some SCN5A gene mutations ...
    https://medlineplus.gov/genetics/gene/scn5a - Genetics
  5. Romano-Ward syndrome 
    ... on PubMed Vincent GM. The Long QT and Brugada syndromes: causes of unexpected syncope and sudden cardiac death ...
    https://medlineplus.gov/genetics/condition/romano-ward-syndrome - Genetics
  6. PRKAG2 gene 
    ... Hong K, Santana O, Brugada P, Brugada J, Brugada R. Familial pseudo-Wolff-Parkinson-White syndrome. J Cardiovasc Electrophysiol. 2006 Jul;17(7):724- ...
    https://medlineplus.gov/genetics/gene/prkag2 - Genetics
  7. Short QT syndrome 
    ... on PubMed or Free article on PubMed Central Brugada R, Hong K, Cordeiro JM, Dumaine R. Short QT syndrome. CMAJ. 2005 Nov 22;173(11):1349-54. ... term follow-up of patients with short QT syndrome. J Am Coll Cardiol. 2011 Aug 2;58(6):587-95. doi: 10.1016/j.jacc.2011. ...
    https://medlineplus.gov/genetics/condition/short-qt-syndrome - Genetics
  8. Jervell and Lange-Nielsen syndrome 
    ... syncope) and sudden death. Jervell and Lange-Nielsen syndrome is uncommon; it affects an estimated 1.6 to 6 per 1 million people worldwide. This ... E, Denjoy I. The Jervell and Lange-Nielsen syndrome: natural history, molecular ... 2006 Feb 14;113(6):783-90. doi: 10.1161/CIRCULATIONAHA.105.592899. ...
    https://medlineplus.gov/.../jervell-and-lange-nielsen-syndrome - Genetics
  9. KCNQ1 gene 
    ... Enfante E, Brugada P, Sachse F, Sanguinetti MC, Brugada R. De novo KCNQ1 mutation responsible for atrial fibrillation and short QT syndrome in utero. Cardiovasc Res. 2005 Dec 1;68( ...
    https://medlineplus.gov/genetics/gene/kcnq1 - Genetics
  10. CDKN1C gene 
    ... R, Camporeale A, Coll Vidal M, Partemi S, Brugada R, Bellocci F, Neri G. Mild Beckwith-Wiedemann and severe long-QT syndrome due to deletion of the imprinting center 2 ...
    https://medlineplus.gov/genetics/gene/cdkn1c - Genetics