A Prospective and Retrospective Registry and Biomarker Study to Evaluate the Natural History of Pediatric Patients with Cardiomyopathy due to MYBPC3 Mutations

Study category: Pediatrics

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Description

This is a natural history study.

Details
Age

Child

Eligibility

Children with a type of cardiomyopathy caused by a specific genetic mutation (MYBPC3 mutation) may be included in this research study.

Type of Study

Observational

Locations

Childrens Hospital Colorado

Principal Investigator
Stephanie Nakano,  MD

Stephanie Nakano, MD

Study ID

Protocol Number: 21-4206

Categories

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