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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
Duplicación Rara del Gen DMD en un Niño Libanés con Distrofia Muscular de Duchenne
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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