hypertrophic cardiomyopathy 6

A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the gene encoding the gamma-2 regulatory subunit of AMP-activated protein kinase (PRKAG2).

Signs and symptoms

• Shortened PR interval
• Prolonged QRS complex
• Hypertrophic cardiomyopathy
• Myofiber disarray
• Asymmetric septal hypertrophy
• Congestive heart failure
• Palpitations
• Sinus bradycardia
• Wolff-Parkinson-White syndrome
• Ventricular preexcitation

Also known as: CMH6; cardiomyopathy, familial hypertrophic 6