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Results 1 - 10 of 18 for Brugada syndrome 2
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  1. Brugada syndrome 
    ... article on PubMed Central Francis J, Antzelevitch C. Brugada syndrome. Int J Cardiol. 2005 May 25;101(2):173-8. doi: 10.1016/j.ijcard.2004. ... 3. Citation on PubMed Li A, Behr ER. Brugada syndrome: an update. Future Cardiol. 2013 Mar;9(2):253-71. doi: 10.2217/fca.12.82. ...
    https://medlineplus.gov/genetics/condition/brugada-syndrome - Genetics
  2. SCN5A gene 
    ... of disease: current understanding and future challenges in Brugada syndrome. Nat Clin Pract Cardiovasc Med. 2005 Aug;2(8):408-14. doi: 10.1038/ncpcardio0268. Citation ...
    https://medlineplus.gov/genetics/gene/scn5a - Genetics
  3. 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 on chromosome 11p. Eur J Hum Genet. 2013 ...
    https://medlineplus.gov/genetics/gene/cdkn1c - Genetics
  4. 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):724-32. doi: 10.1111/j.1540-8167.2006.00485.x. Citation on PubMed
    https://medlineplus.gov/genetics/gene/prkag2 - Genetics
  5. KCNH2 gene 
    ... on PubMed Hong K, Bjerregaard P, Gussak I, Brugada R. Short QT ... BP. Mechanistic basis for type 2 long QT syndrome caused by KCNH2 mutations that ...
    https://medlineplus.gov/genetics/gene/kcnh2 - Genetics
  6. 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
  7. Progressive familial heart block 
    ... is the prevailing phenotype in carriers of a Brugada syndrome SCN5A mutation. J Cardiovasc Electrophysiol. 2006 Mar;17( ... CR. Sodium channel beta1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans. J Clin ...
    https://medlineplus.gov/.../progressive-familial-heart-block - Genetics
  8. Jervell and Lange-Nielsen syndrome 
    ... 1 Genetic Testing Registry: Jervell and Lange-Nielsen syndrome 2 Jervell and Lange-Nielsen syndrome National Organization for ... NIELSEN SYNDROME 1; JLNS1 JERVELL AND LANGE-NIELSEN SYNDROME 2; JLNS2 PubMed Mizusawa Y, Horie M, Wilde AA. ...
    https://medlineplus.gov/.../jervell-and-lange-nielsen-syndrome - Genetics
  9. CACNA1C gene 
    ... This Health Condition MedlinePlus Genetics provides information about Brugada syndrome More About This Health Condition Variants in the ... of the gene than those that cause Timothy syndrome. While these CACNA1C gene variants alter CaV1.2 channels and calcium channel flow, it is unclear ...
    https://medlineplus.gov/genetics/gene/cacna1c - Genetics
  10. Syncope (Fainting) (Heart Rhythm Society)  
    Fainting/Related Issues ... Fainting ... Heart Rhythm Society ... Fainting (syncope) is a sudden transient loss of consciousness. It most often happens when the blood ...
    https://upbeat.org/early-warning-signs/syncope - External Health Links
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