Dilated cardiomyopathy 1A

Familial dilated cardiomyopathy with conduction defect due to LMNA mutation is a rare familial dilated 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 and elevated serum creatine kinase.

Also known as: CDCD1, LMNA familial isolated dilated cardiomyopathy, cardiomyopathy dilated with conduction defect type 1, cardiomyopathy, dilated, type 1A, dilated cardiomyopathy 1A, dilated cardiomyopathy type 1A, familial dilated cardiomyopathy with conduction defect due to LMNA mutation, familial isolated dilated cardiomyopathy caused by mutation in LMNA

10 clinical trials for this condition and its sub-types, 2 tagged with Dilated cardiomyopathy 1A itself.