Familial progressive cardiac conduction defect

Disease Export to PDF
Name:
Familial progressive cardiac conduction defect
Description:
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.
ORPHAcode:
871
Synonyms:
Familial Lenègre disease
Familial Lev disease
Familial Lev-Lenègre disease
Familial PCCD
Familial progressive heart block
Hereditary bundle branch defect
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Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14