Cardiac Involvement Classification and Therapeutic Management in Patients with Duchenne Muscular Dystrophy

نویسندگان

  • Abdallah Fayssoil
  • Soumeth Abasse
  • Katy Silverston
چکیده

Duchenne muscular dystrophy (DMD) is an inherited myogenic disorder due to mutations in the dystrophin gene on chromosome Xp21.1. The clinical picture included peripheral muscle weakness, cardiomyopathy and chronic respiratory insufficiency. In this paper, the authors review cardiac involvement in patients with DMD, propose a cardiac impairment classification and discuss therapeutic management options.

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عنوان ژورنال:

دوره 4  شماره 

صفحات  -

تاریخ انتشار 2017