Article

Mutation identification and prediction for severe cardiomyopathy in Alström syndrome, and review of the literature for cardiomyopathy

2022-04-13

Abstract excerpt

<title>Abstract</title> <p>Objective: Alström syndrome (ALMS1)(OMIM# 203800) is a rare autosomal recessive genetic disorder. Dilated cardiomyopathy (DCM) is one of the well-recognized feature of the syndrome ranging from sudden-onset infantile DCM, to adult onset cardiomyopathy, sometimes of the restrictive hypertrophic form with a poor prognosis. We aimed to evaluate severe cardiomyopathy in Alström syndrome in...

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Literature Corpus work: 7e8b656a-26ca-50af-8ef6-017c61b3bf05
DOI: 10.21203/rs.3.rs-1502633/v1

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