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An Instance of Hypokalemic Periodic Paralysis in Adolescent Brothers: A Case Report
Hypokalemic periodic paralysis (HypoPP) is a rare autosomal dominant disease caused by mutations in either calcium or sodium transmembrane voltage-gated ion channels of skeletal muscle or endoplasmic reticulum. Most cases of HypoPP are associated with a mutation in the gene encoding a calcium channe...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Cureus
2023
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10434723/ https://www.ncbi.nlm.nih.gov/pubmed/37601992 http://dx.doi.org/10.7759/cureus.42082 |