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1. A rare cause of mixed hypertrophic and dilated phenotype cardiomyopathy – the MELAS syndrome

Author

Casian Mihnea, Dragotoiu Nic, Onciul Sebastian, Popescu Bogdan A., and Jurcuţ Ruxandra

Subjects
melas, mitochondrial disease, hereditary cardiomyopathy, genetic test, boală mitocondrială, cardiomiopatie ereditară, testare genetică, Internal medicine, RC31-1245
Abstract

MELAS is a systemic hereditary condition that can present as hypertrophic or mixed hypertrophic and dilated phenotype cardiomyopathy in young individuals, although a late-onset form is also described in the literature. Genetic testing is essential for correct diagnosis and appropriate management.

Published
2023
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