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.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5345647PMC
http://dx.doi.org/10.3233/JND-160194DOI Listing

Publication Analysis

Top Keywords

cardiac involvement
8
therapeutic management
8
duchenne muscular
8
muscular dystrophy
8
involvement classification
4
classification therapeutic
4
management patients
4
patients duchenne
4
dystrophy duchenne
4
dystrophy dmd
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!