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Rev. méd. Maule ; 37(2): 63-69, dic. 2022. ilus
Article in Spanish | LILACS | ID: biblio-1428507

ABSTRACT

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.


Subject(s)
Humans , Male , Adult , Muscular Dystrophy, Duchenne/diagnosis , Muscular Dystrophy, Duchenne/genetics , Muscular Dystrophy, Duchenne/therapy , Cardiomyopathy, Dilated , Dystrophin/genetics , Muscular Dystrophy, Duchenne/classification , Muscular Dystrophy, Duchenne/physiopathology , Diagnosis, Differential , Heart Failure
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