The Pediatric Cardiomyopathy Registry was established to describe the epidemiologic features and clinical course of selected cardiomyopathies in patients aged 18 years or younger and to promote the development of etiology-specific treatments.

The Pediatric Cardiomyopathy Registry was funded from 1994 to 2010 by the National Heart, Lung, and Blood Institute.

For more information on the Pediatric Cardiomyopathy Registry,
please contact JJ McGill at 617-923-7747 x231.