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Primary Hypokalemic Periodic Paralysis: Long-term Management and Complications in a Child
Hypokalemic periodic paralysis (HPP) is a rare genetically determined neuromuscular disorder caused by mutation in skeletal muscles calcium and sodium channels. It presents with recurrent episodes of flaccid paralysis. A 9-year-old girl presented with recurrent episodic flaccid quadriparesis with co...
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| Publicado no: | J Pediatr Neurosci |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Wolters Kluwer - Medknow
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7519733/ https://ncbi.nlm.nih.gov/pubmed/33042247 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/jpn.JPN_101_19 |
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