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Hyperkalemic Periodic Paralysis: Case Report with a SCNA4 Gene Mutation and Literature Review

Hyperkalemic periodic paralysis is a rare musculoskeletal disorder characterized by episodic muscle weakness associated with hyperkalemia. It is a channelopathy associated with point mutations in the SCNA4 gene, with an autosomal dominant pattern of inheritance. We report the case of a 39-year-old p...

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Detalles Bibliográficos
Autores principales:	Quiroga-Carrillo, Manuela, Correa-Arrieta, Cristian, Ortiz-Corredor, Fernando, Suarez-Obando, Fernando
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Hindawi 2020
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7585666/ https://www.ncbi.nlm.nih.gov/pubmed/33123387 http://dx.doi.org/10.1155/2020/8843410

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