Brugada Syndrome: A rare genetic disorder characterized by heart rhythm abnormalities which can result in sudden death if untreated. The condition may be inherited in some cases. The mean age of sudden death is 40 years of age. More detailed information about the symptoms, causes, and treatments of Brugada Syndrome is available below.
See full list of 8 symptoms of Brugada Syndrome
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Brugada Syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Brugada Syndrome, or a subtype of Brugada Syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Brugada Syndrome as a "rare disease".
Source - Orphanet
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