Question

The variant identified as the cause of HCM in the patient is ____________. (select all that...

The variant identified as the cause of HCM in the patient is ____________. (select all that apply)
autosomal
X-linked
Y-linked
dominant
recessive

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Answer #1

Autosomal and dominant

Familial hypertrophic cardiomyopathy (HCM) is an autosomal trait, meaning that having only one changed or mutated copy of the responsible gene in each cell is enough to cause this disease. It is causes by mutation in sacromere protein gene.

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