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Rev. méd. Maule ; 37(2): 63-69, dic. 2022. ilus
Artigo em Espanhol | LILACS | ID: biblio-1428507

RESUMO

Neuromuscular diseases represent a rare cause of dilated myocardiopathy, among them Duchenne muscular dystrophy is the most common. Transthoracic echocardiography and cardiac magnetic resonance imaging can assess cardiac involvement early. The case of a patient diagnosed with Duchenne muscular dystrophy who develops cardiac involvement during cardiology follow-up is presented below.


Assuntos
Humanos , Masculino , Adulto , Distrofia Muscular de Duchenne/diagnóstico , Distrofia Muscular de Duchenne/genética , Distrofia Muscular de Duchenne/terapia , Cardiomiopatia Dilatada , Distrofina/genética , Distrofia Muscular de Duchenne/classificação , Distrofia Muscular de Duchenne/fisiopatologia , Diagnóstico Diferencial , Insuficiência Cardíaca
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