Familial atrial fibrillation

From WikiMD.org
Jump to navigation Jump to search

Familial Atrial Fibrillation

Familial Atrial Fibrillation (pronounced: fuh-MILL-ee-ul AY-tree-ul fib-ril-LAY-shun) is a genetic disorder that disrupts the heart's normal rhythm, leading to a rapid and irregular heartbeat. It is a type of Atrial Fibrillation that runs in families.

Etymology

The term 'Familial Atrial Fibrillation' is derived from the Latin words 'familia' meaning family, 'atrium' referring to the upper chambers of the heart, and 'fibrillare' meaning to quiver.

Definition

Familial Atrial Fibrillation is a condition characterized by chaotic electrical activity in the heart's upper chambers (the atria), resulting in a fast and irregular heartbeat (arrhythmia). It is a subtype of Atrial Fibrillation that is inherited within families, suggesting a genetic predisposition.

Symptoms

Symptoms of Familial Atrial Fibrillation can include palpitations, shortness of breath, fatigue, and sometimes, it may be asymptomatic.

Causes

Familial Atrial Fibrillation is caused by genetic mutations. These mutations often affect genes involved in the production of proteins that play key roles in the heart's electrical system.

Diagnosis

Diagnosis of Familial Atrial Fibrillation is based on the patient's family history, symptoms, and results from tests such as an Electrocardiogram (ECG) or Holter Monitor.

Treatment

Treatment for Familial Atrial Fibrillation can include medications, lifestyle changes, and sometimes procedures such as Catheter Ablation or Cardioversion.

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