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Early onset development of hypertrophic cardiomyopathy in less than 1 year in a patient with familial Friedrich's ataxia: Case report

Friedreich's ataxia (FRDA) is a neurodegenerative disease characterized by progressive ataxia, dysarthria, sensory loss. While neurological symptoms are prominent, cardiac manifestations significantly contribute to mortality. Cardiomyopathy in Friedreich's disease results from mitochondrial dysfunct...

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Principais autores: Yasmine Ouaddouh, MD, Salma Bouyaddid, MD, Zakaria Bazid, MD, PhD, Nabila Ismaili, MD, PhD, Noha El Ouafi, MD, PhD
Formato: Artigo
Idioma:Inglês
Publicado em: Elsevier 2025-06-01
coleção:Radiology Case Reports
Assuntos:
Hypertrophic cardiomyopathy
Friedreich ataxia
Mitochondrial dysfunction
Mortality
Acesso em linha:http://www.sciencedirect.com/science/article/pii/S1930043325002158
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