Familial atrial fibrillation

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Familial atrial fibrillation is a rare genetically heterogenous cardiac disease characterized by erratic activation of the atria with an irregular ventricular response in various members of a single family. It may be asymptomatic or associated with palpitations dyspnea and light-headedness. Concomitant rhythm disorders and cardiomyopathies are frequently reported.

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview. Reference: Access aggregated data from Orphanet at Orphadata. Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version July 2024

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Familial atrial fibrillation?

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Advocacy Organizations

Team Titin

Team Titin, Inc.'s mission is to serve those living with, caring for, or researching titin (TTN) related muscle and heart disorders. To achieve this mission, we focus on four key pillars: Connection, Advocacy, Care, and Research.

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Clinical Trials

For a list of clinical trials in this disease area, please click here.