Sökning: "Familial hypertrophic cardiomyopathy"
Hittade 2 avhandlingar innehållade orden Familial hypertrophic cardiomyopathy.
1. Early Cardiovascular Changes of Familial Hypertrophic Cardiomyopathy in the Young
Sammanfattning : Familial hypertrophic cardiomyopathy (HCM) is the most common inherited heart disease, transmitted in an autosomal dominant fashion, i.e. 50% risk for transmission of the disease-causing mutation to each child of the affected family. LÄS MER
2. Hypertrophic cardiomyopathy in Northern Sweden : with special emphasis on molecular genetics
Sammanfattning : Hypertrophic cardiomyopathy (HCM) is a heterogeneous, often familial disease, characterized by cardiac hypertrophy, predominantly affecting the interventricular septum. To date, no study has systematically analysed the genetic and phenotypic aspects of the disease in a Swedish population. LÄS MER
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