
pmid: 17977476
Abstract The role of familial disease in childhood dilated cardiomyopathy is unknown. A novel mutation in the cardiac Troponin C gene has been identified recently in a family with dilated cardiomyopathy. Here we present a subsequent case of dilated cardiomyopathy occurring in a child from the same family, and emphasise the implications for future screening and counselling.
Cardiomyopathy, Dilated, Male, Biopsy, Myocardium, DNA Mutational Analysis, DNA, Myocardial Contraction, Severity of Illness Index, Echocardiography, Doppler, Color, Pedigree, Electrocardiography, Child, Preschool, Mutation, Heart Transplantation, Humans, Genetic Predisposition to Disease, Troponin C, Follow-Up Studies
Cardiomyopathy, Dilated, Male, Biopsy, Myocardium, DNA Mutational Analysis, DNA, Myocardial Contraction, Severity of Illness Index, Echocardiography, Doppler, Color, Pedigree, Electrocardiography, Child, Preschool, Mutation, Heart Transplantation, Humans, Genetic Predisposition to Disease, Troponin C, Follow-Up Studies
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