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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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| Publicat a: | Neurosciences (Riyadh) |
|---|---|
| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Riyadh : Armed Forces Hospital
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8015512/ https://ncbi.nlm.nih.gov/pubmed/31380823 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.17712/nsj.2018.3.20180005 |
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