... J, Straub V. Does delta-sarcoglycan-associated autosomal-dominant cardiomyopathy exist? Eur J Hum Genet. 2009 Sep;17( ...

... 80 to 90 percent of cases, familial dilated cardiomyopathy is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder. In most cases, an ... cardiomyopathy. (This situation is known as reduced penetrance.) Other ...

... MYOZ2 NEXN PLN TCAP TPM1 VCL Familial hypertrophic cardiomyopathy is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder. Rarely, both copies of ... hypertrophic cardiomyopathy is not inherited. Its cause is complex and ...

... Matthias P, Saffitz JE, McKenna WJ. A novel dominant mutation in plakoglobin causes arrhythmogenic right ventricular cardiomyopathy. Am J Hum Genet. 2007 Nov;81(5): ...

... ACTC1 This condition is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder. Cardiomyopathy, restrictive RCM Genetic Testing Registry: Familial restrictive cardiomyopathy ...

... muscle disease, and a heart disorder called hypertrophic cardiomyopathy. Several CAV3 gene mutations have been ... This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ...

... isolated hyperCKemia, and a heart disorder called hypertrophic cardiomyopathy. Several CAV3 gene mutations ... This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ...

Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a form of heart disease that usually appears in adulthood. ARVC is a disorder of the myocardium, which is the ...