Duchenne Muscular Dystrophy Presenting as Incidental Hyper-Transaminasasemia in a Two-Month-Old Male

Duchenne's muscular dystrophy (DMD) is a debilitating X-linked recessive disorder of dystrophin gene expression that culminates in the downregulation of dystrophin in cardiac and skeletal muscle. As a result, there is progressive muscle weakness, fibrosis, and atrophy. The skeletal and cardiac...

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Detalles Bibliográficos
Autores principales: Chibuzo, Uzoego N, Bruman, Madeline, Holguin, Ariela, Bangaru, Babu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10049938/
https://www.ncbi.nlm.nih.gov/pubmed/37007358
http://dx.doi.org/10.7759/cureus.35498

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10049938/
https://www.ncbi.nlm.nih.gov/pubmed/37007358
http://dx.doi.org/10.7759/cureus.35498

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