dilated cardiomyopathy 2G

A dilated cardiomyopathy that is characterized by early-onset severe dilated cardiomyopathy that progresses rapidly to heart failure in the neonatal period without evidence of intervening hypertrophy and that has_material_basis_in homozygous or compound hetero

A dilated cardiomyopathy that is characterized by early-onset severe dilated cardiomyopathy that progresses rapidly to heart failure in the neonatal period without evidence of intervening hypertrophy and that has_material_basis_in homozygous or compound heterozygous mutation in the LMOD2 gene on chromosome 7q31.

Signs and symptoms

• Cerebral hemorrhage
• Myofiber disarray
• Paroxysmal ventricular tachycardia
• Complete right bundle branch block
• Monomorphic ventricular tachycardia
• Severely reduced left ventricular ejection fraction
• Left atrial enlargement
• Tachycardia
• Aortic regurgitation
• Mitral regurgitation