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Updated: Feb 4, 2026

Measurements of Motor Function and Other Clinical Outcome Parameters in Ambulant Children with Duchenne Muscular Dystrophy
Published on: January 12, 2019
Rare DMD Gene Duplication in a Lebanese Child With Duchene Muscular Dystrophy
Nada Assaf1, Jeanette El Hajj1, Jana Doghman1
1Department of Pathology and Laboratory Medicine American University of Beirut Medical Center Beirut Lebanon.
Abstract:
A five-year-old boy with clinical features of Duchenne muscular dystrophy was found to have a rare de novo DMD exon 2-9 duplication. Reporting such atypical duplications improves genotype-phenotype interpretation and highlights the need for multidisciplinary care, particularly in resource-limited settings.
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