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- W174097838 abstract "Hypertrophic cardiomyopathy typically presents as an isolated cardiac lesion. Transient hypertrophic cardiomyopathy in infancy has been described as a result of exposure to maternal metabolic disorders or to corticosteroids. In addition, hypertrophic cardiomyopathy has been described in association with genetic syndromes and, in rare cases, as a primary lesion associated with other congenital heart defects. We describe the unusual association of hypertrophic cardiomyopathy and complete atrioventricular canal defect in an infant with trisomy 21." @default.
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- W174097838 date "2000-01-01" @default.
- W174097838 modified "2023-09-23" @default.
- W174097838 title "Unusual association of hypertrophic cardiomyopathy with complete atrioventricular canal defect and Down syndrome." @default.
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