Conditions / Genetic
dilated cardiomyopathy 3B
info · Genetic · ICD-10: I42.0
A dilated cardiomyopathy that has_material_basis_in mutation in the dystrophin (DMD) gene encoding dystrophin on chromosome Xp21.
Signs and symptoms
- Elevated circulating CK-MB concentration
- Increased left ventricular end-diastolic volume
- Dilated cardiomyopathy
- Increased variability in muscle fiber diameter
Also known as: CMD3B; DMD-related dilated cardiomyopathy; X-linked dilated cardiomyopathy; XLCM