Moroccan consanguineous family with Becker myotonia and review

Myotonia congenita is a genetic muscle disorder characterized by clinical and electrical myotonia, muscle hypertrophy, and stiffness. It is inherited as either autosomal-dominant or –recessive, known as Thomsen and Becker diseases, respectively. These diseases are distinguished by the severity of th...

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Detalles Bibliográficos
Autores principales: Ratbi, Ilham, Elalaoui, Siham Chafai, Escudero, Adela, Kriouile, Yamina, Molano, Jesus, Sefiani, Abdelaziz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2011
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3271475/
https://www.ncbi.nlm.nih.gov/pubmed/22346025
http://dx.doi.org/10.4103/0972-2327.91963

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3271475/
https://www.ncbi.nlm.nih.gov/pubmed/22346025
http://dx.doi.org/10.4103/0972-2327.91963

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