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