Familial dilated cardiomyopathy with conduction defect due to LMNA mutation

Orpha code: 300751OMIM code: 115200

Definition

A rare familial cardiomyopathy characterized by left ventricular enlargement and/or reduced systolic function preceded or accompanied by significant conduction system disease and/or arrhythmias including bradyarrhythmias, supraventricular or ventricular arrhythmias. Disease onset is usually in early to mid-adulthood. Sudden cardiac death may occur and may be the presenting symptom. In some cases, it is associated with skeletal myopathy.

Disease data
Classification

Disease

ORPHA code
300751
OMIM code
115200
ICD10 code
I42.0
ICD11 code
-

No additional description.

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