Congenital Muscular Dystrophy Due to Merosin Deficiency: Report of a New Mutation

Congenital muscular dystrophy due to merosin deficiency is one of the most common congenital muscular dystrophies. It is characterized by a LAMA2 gene mutation and causes varied clinical symptoms depending on the type of presentation. In this case report, we identified the importance of the medical...

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Detalles Bibliográficos
Autores principales: Herrera Malpica, Wilmer Santiago, Ortiz-Corredor, Fernando, Sanchez Peñarete, Diana, Muñetones Hernández, Paula Vanessa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10321457/
https://www.ncbi.nlm.nih.gov/pubmed/37416022
http://dx.doi.org/10.7759/cureus.39988

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10321457/
https://www.ncbi.nlm.nih.gov/pubmed/37416022
http://dx.doi.org/10.7759/cureus.39988

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