Calpainopathy (Leyden-Mobius Limb-Girdle Muscular Dystrophy Type 2A Phenotype) and Dysferlinopathy (Miyoshi Distal Myopathy Limb-Girdle Muscular Dystrophy Type 2B Phenotype) of Preadolescent Onset: Case Reports of Two Male Filipinos

Limb-girdle muscle dystrophy (LGMD) is the fourth most common genetic cause of muscle weakness, with LGMD type 2A (LGMD2A) being one of the most common adult-onset muscular dystrophies presenting with limb-girdle weakness, while LGMD type 2B (LGMD2B) being the most common distal myopathy. This study...

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Detalles Bibliográficos
Autores principales: Quilacio, Joanna May S, Rosales, Raymond L, Ampil, Encarnita R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8853928/
https://www.ncbi.nlm.nih.gov/pubmed/35198268
http://dx.doi.org/10.7759/cureus.21353

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8853928/
https://www.ncbi.nlm.nih.gov/pubmed/35198268
http://dx.doi.org/10.7759/cureus.21353

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