Familial progressive cardiac conduction defect

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Familial progressive cardiac conduction defect

Synonyms: Familial Lenègre disease | Familial Lev disease | Familial Lev-Lenègre disease | Familial PCCD | Familial progressive heart block | Hereditary bundle branch defect

A genetic cardiac rhythm disease that may progress to complete atrioventricular (AV) block. The disease is either asymptomatic or manifests as dyspnea dizziness syncope abdominal pain heart failure or sudden death.

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 October 2023.

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Familial progressive cardiac conduction defect?

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Advocacy Organizations

My Faulty Gene

My Faulty Gene is a nonprofit organization which provides information and assistance to any individual whose family medical history suggests genetic testing might be helpful in identifying an increased risk of disease due to a genetic mutation. We believe that everyone in need of genetic testing should have access to it.

Clinical Trials

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