Hypertrophic cardiomyopathy (HCM3)

(Ragdoll) more
Disease
autosomal dominant
Heredity
HCM is characterised by an increased left ventricular mass due to an increase in wall thickness of the heart, with papillary muscle hypertrophy and systolic anterior motion of the Mitral valves. Subsequently, hypertrophy of the left heart chamber results in cardiac weakness and ultimately in heart failure.
Test duration
TaqMan SNP Assay
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