However, mutations in G4.5 result in a wide clinical spectrum, which includes apparent classic DCM, hypertrophic DCM, endocardial fibroelastosis, or left ventricular noncompaction, with or without ...

harthosp.org Non-compaction cardiomyopathy (NCCM) is typified by deep invaginations of the myocardium and is caused by an arrest of normal myocardial morphogenesis. NCCM was once considered rare, but ...

The Inherited Arrhythmia and Cardiomyopathy Clinic at Baylor Medicine offers a multidisciplinary team to evaluate, diagnose and treat patients with inherited arrhythmias and cardiomyopathies.