Familial progressive cardiac conduction defect

Get in touch with RARE Concierge.

Contact RARE Concierge

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 July 2024

Newly diagnosed with
Familial progressive cardiac conduction defect?

Our RARE Concierge Services Guides are available to assist you by providing information, resources and connections as you navigate your rare disease journey.

Get Concierge Help

Clinical Trials

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