Hypokalemic periodic paralysis; two different genes responsible for similar clinical manifestations

Primary hypokalemic periodic paralysis (HOKPP) is an autosomal dominant disorder manifesting as recurrent periodic flaccid paralysis and concomitant hypokalemia. HOKPP is divided into type 1 and type 2 based on the causative gene. Although 2 different ion channels have been identified as the molecul...

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Detalles Bibliográficos
Autores principales: Kim, Hunmin, Hwang, Hee, Cheong, Hae Il, Park, Hye Won
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Pediatric Society 2011
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3254894/
https://www.ncbi.nlm.nih.gov/pubmed/22253645
http://dx.doi.org/10.3345/kjp.2011.54.11.473

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3254894/
https://www.ncbi.nlm.nih.gov/pubmed/22253645
http://dx.doi.org/10.3345/kjp.2011.54.11.473

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