Case Report: The Genetic Diagnosis of Duchenne Muscular Dystrophy in the Middle East

Case Report: The Genetic Diagnosis of Duchenne Muscular Dystrophy in the Middle East

The timely and accurate genetic diagnosis of Duchenne muscular dystrophy (DMD) enables prompt initiation of disease management and genetic counseling and optimal patient care. Despite the existence of best practice guidelines for the diagnosis of DMD, implementation of these recommendations in diffe...

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Bibliographic Details
Main Authors: Fouad Alghamdi, Asmaa Al-Tawari, Hadil Alrohaif, Walaa Alshuaibi, Hicham Mansour, Annemieke Aartsma-Rus, André Mégarbané
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-09-01
Series:Frontiers in Pediatrics
Subjects:
case report
diagnostic delay
DMD
genetic diagnosis
neuromuscular disorder
Online Access:https://www.frontiersin.org/articles/10.3389/fped.2021.716424/full

Internet

https://www.frontiersin.org/articles/10.3389/fped.2021.716424/full

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