Conditions / Cardiovascular
hypertrophic cardiomyopathy 8
info · Cardiovascular
A familial hypertrophic cardiomyopathy that has_material_basis_in homozygous or heterozygous mutation in the MYL3 gene.
Signs and symptoms
- T-wave inversion
- Hypertrophic cardiomyopathy
- Left ventricular hypertrophy
- Ventricular fibrillation
- Cardiac arrest
- Left atrial enlargement
- Restrictive cardiomyopathy
- Endocardial fibrosis
- Palpitations
- Sudden cardiac death
Also known as: cardiomyopathy hypertrophic mid-left ventricular chamber type 1; cardiomyopathy, familial hypertrophic, 8