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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 and related Studies are funded from 1994 to 2016 by the National Heart, Lung, and Blood Institute.

For more information on the Pediatric Cardiomyopathy Registry,
please contact Nicole Turcotte at 617-972-3045.

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