Histiocytoid cardiomyopathy

Histiocytoid cardiomyopathy is an arrhythmogenic disorder characterized by cardiomegaly, severe cardiac arrhythmias or sudden death, and the presence of histiocyte-like cells within the myocardium.

Also known as: Arachnocytosis of the myocardium, Purkinje cell hamartoma, congenital cardiomyopathy, foamy myocardial transformation of infancy, histiocytoid cardiomyopathy, infantile cardiomyopathy with histiocytoid change, infantile xanthomatous cardiomyopathy, isolated Cardiac lipidosis

23 clinical trials for this condition and its sub-types.