Possibly: This is a large, diverse topic. There is a familial basis for some patients with Wolff-Parkinson-White syndrome. Hypertrophic cardiomyopathy is typically a genetic disease and some cohorts have increased prevalence of svt and wpw. There are mitochondrial mutations that appear to have increased prevalence of svt.
Answered 9/8/2017
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2 doctors weighed in across 2 answers
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