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Phenotypical Variation with Same Genetic Mutation in Familial Hypokalemic Periodic Paralysis
Hypokalemic periodic paralysis is a genetic neuromuscular disorder characterized by episodes of painless muscle paralysis associated with low serum potassium, exclusively, during the attack. This may be precipitated by heavy exercise, fasting, or high-carbohydrate meals. We report two siblings, pres...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Medknow Publications & Media Pvt Ltd
2018
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6057184/ https://www.ncbi.nlm.nih.gov/pubmed/30090141 http://dx.doi.org/10.4103/jpn.JPN_44_17 |