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The clinical course of Duchenne muscular dystrophy in the corticosteroid treatment era: a systematic literature review

Abstract Background Duchenne muscular dystrophy (DMD) is a severe rare progressive inherited neuromuscular disorder, leading to loss of ambulation (LOA) and premature mortality. The standard of care for patients with DMD has been treatment with corticosteroids for the past decade; however a synthesi...

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Hauptverfasser: Shelagh M. Szabo, Renna M. Salhany, Alison Deighton, Meagan Harwood, Jean Mah, Katherine L. Gooch
Format: Artigo
Sprache:Inglês
Veröffentlicht: BMC 2021-05-01
Schriftenreihe:Orphanet Journal of Rare Diseases
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Online-Zugang:https://doi.org/10.1186/s13023-021-01862-w
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