Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 8 of 8 for Brugada syndrome
Did you mean uganda syndrome?
  1. 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
  2. CACNA1C gene 
    ... This Health Condition MedlinePlus Genetics provides information about Brugada syndrome More About This Health Condition Variants in the ...
    https://medlineplus.gov/genetics/gene/cacna1c - Genetics
  3. TRPM4 gene 
    ... This Health Condition MedlinePlus Genetics provides information about Brugada syndrome More About This Health Condition calcium-activated non- ...
    https://medlineplus.gov/genetics/gene/trpm4 - Genetics
  4. HCN4 gene 
    ... This Health Condition MedlinePlus Genetics provides information about Brugada syndrome More About This Health Condition MedlinePlus Genetics provides ...
    https://medlineplus.gov/genetics/gene/hcn4 - Genetics
  5. KCNH2 gene 
    ... on PubMed Hong K, Bjerregaard P, Gussak I, Brugada R. Short QT syndrome and atrial fibrillation caused by mutation in KCNH2. ...
    https://medlineplus.gov/genetics/gene/kcnh2 - 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. 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
  8. 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