National Organization for Rare Disorders, Inc.
It is possible that the main title of the report Brugada Syndrome is not the name you expected.
Brugada syndrome is a rare inherited cardiovascular disorder characterized by disturbances affecting the electrical system of the heart. The main symptom is irregular heartbeats and, without treatment, may potentially result in sudden death. In some cases, no symptoms may precede sudden death. Brugada Syndrome typically begins onset in adulthood and follows autosomal dominant inheritance. The prevalence rate of the disease is currently unknown due to its recent identification.
The normal heart has four chambers. The two upper chambers are known as the atria and the two lower chambers are known as the ventricles. Electrical impulses cause the heart to beat. In individuals with Brugada syndrome, the electrical impulses between the ventricles become uncoordinated (ventricular fibrillation) resulting in decreased blood flow. Decreased blood flow to the brain and heart may result in fainting or sudden death.
Brugada syndrome is named by the Spanish cardiologists Pedro Brugada and Josep Brugada who reported it as a distinct clinical syndrome in 1992.
American Heart Association
- 7272 Greenville Avenue
- Dallas, TX 75231
- Tel: (214)784-7212
- Fax: (214)784-1307
- Tel: (800)242-8721
- Email: Review.email@example.com
- Website: http://www.heart.org
Genetic and Rare Diseases (GARD) Information Center
- PO Box 8126
- Gaithersburg, MD 20898-8126
- Tel: (301)251-4925
- Fax: (301)251-4911
- Tel: (888)205-2311
- Website: http://rarediseases.info.nih.gov/GARD/
Ramon Brugada Senior Foundation
- Pic de Peguera 15
- Girona, 17003
- Tel: 34 972 183366
- Fax: 34 972 183367
- Email: firstname.lastname@example.org
- Website: http://www.brugada.org/foundation/foundation.html
Sudden Arrhythmia Death Syndromes Foundation
- 508 E. South Temple
- Suite 202
- Salt Lake City, UT 84102
- Tel: (801)531-0937
- Fax: (801)531-0945
- Tel: (800)786-7723
- Email: email@example.com
- Website: http://www.sads.org
For a Complete Report
This is an abstract of a report from the National Organization for Rare Disorders (NORD). For a full-text version of this report, go to www.rarediseases.org and click on Rare Disease Database under "Rare Disease Information".
The information provided in this report is not intended for diagnostic purposes. It is provided for informational purposes only.
It is possible that the title of this topic is not the name you selected. Please check the Synonyms listing to find the alternate name(s) and Disorder Subdivision(s) covered by this report.
This disease entry is based upon medical information available through the date at the end of the topic. Since NORD's resources are limited, it is not possible to keep every entry in the Rare Disease Database completely current and accurate. Please check with the agencies listed in the Resources section for the most current information about this disorder.
Last Updated: 2/7/2013
Copyright 2013 National Organization for Rare Disorders, Inc.
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