Hypokalemic periodic paralysis due to CACNA1S gene mutation

Hypokalemic periodic paralysis (HypoPP) is a relatively rare but treatable disorder caused by mutations in the CACNA1S gene. HypoPP patients may experience paralytic episodes associated with hypokalemia and, infrequently, may develop late-onset proximal myopathy. The paralytic attacks are characteri...

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Detalles Bibliográficos
Autores principales: Alhasan, Khalid A., Abdallah, Mohammed S., Kari, Jameela A., Bashiri, Fahad A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Riyadh : Armed Forces Hospital 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8015512/
https://www.ncbi.nlm.nih.gov/pubmed/31380823
http://dx.doi.org/10.17712/nsj.2018.3.20180005

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8015512/
https://www.ncbi.nlm.nih.gov/pubmed/31380823
http://dx.doi.org/10.17712/nsj.2018.3.20180005

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