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...

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Detalles Bibliográficos
Autores principales: Kumar, Sumant, Offiong, Eniang E., Sangita, Sweta, Hussain, Nahin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Case Report
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

Internet

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

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