Cardiac Involvement Classification and Therapeutic Management in Patients with Duchenne Muscular Dystrophy
Abdallah Fayssoil1,2, Soumeth Abasse3, Katy Silverston4
1APHP, Raymond Poincare Hospital, University of Versailles, Garches, France.
Abstract:
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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