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...

Descripción completa

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

Internet

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

Ejemplares similares