Brugada Syndrome

From WikiMD.org
Jump to navigation Jump to search

Brugada Syndrome

Brugada Syndrome (pronounced: broo-GAH-dah sin-drome) is a potentially life-threatening heart rhythm disorder that is sometimes inherited. People with Brugada Syndrome have an increased risk of abnormal heart rhythms from the lower chambers of the heart (ventricles).

Etymology

The syndrome is named after the Brugada brothers, Pedro Brugada and Josep Brugada, Spanish cardiologists who described the syndrome in 1992.

Symptoms

The most common symptom of Brugada Syndrome is a sudden loss of consciousness (syncope). In some cases, the disorder can cause sudden cardiac death.

Causes

Brugada Syndrome is often inherited, but it can also occur as a result of a severe electrolyte imbalance or as a side effect of certain medications.

Diagnosis

Diagnosis of Brugada Syndrome is typically made through an electrocardiogram (ECG), which can detect the abnormal heart rhythms characteristic of the syndrome.

Treatment

Treatment for Brugada Syndrome typically involves the use of an implantable cardioverter defibrillator (ICD), which can correct abnormal heart rhythms.

Related Terms

External links

Esculaap.svg

This WikiMD dictionary article is a stub. You can help make it a full article.


Languages: - East Asian 中文, 日本, 한국어, South Asian हिन्दी, Urdu, বাংলা, తెలుగు, தமிழ், ಕನ್ನಡ,
Southeast Asian Indonesian, Vietnamese, Thai, မြန်မာဘာသာ, European español, Deutsch, français, русский, português do Brasil, Italian, polski