Becker muscular dystrophy
Vol. 164 No. 3 (2025): Vol. 164 Núm. 3 (2025): Vol. 164 Núm. 3 (2025): Septiembre - Diciembre
Case Report
January 31, 2026
February 1, 2026
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Muscular dystrophies are degenerative, X-linked recessive disorders. They are relatively
uncommon, affecting 8 to 10 cases per 100,000 males. The disease is caused by a
mutation in the dystrophin gene, which is responsible for linking actin in the cytoskeleton
to the extracellular matrix in skeletal and cardiac myocytes, the primary organs affected
by the disease. Below is a case presentation of a 13-year-old patient with Becker
muscular dystrophy, confirmed by genetic analysis
Becker muscular dystrophy. (2026). Revista médica (Colegio De Médicos Y Cirujanos De Guatemala), 164(3). https://doi.org/10.36109/pe9nrm33
How to Cite
Becker muscular dystrophy. (2026). Revista médica (Colegio De Médicos Y Cirujanos De Guatemala), 164(3). https://doi.org/10.36109/pe9nrm33