Familial Normokalemic Periodic Paralysis Associated With Mutation in the SCN4A p.M1592V

Familial Normokalemic Periodic Paralysis Associated With Mutation in the SCN4A p.M1592V

Periodic paralysis (PP) is an uncommon inherited disorder causing recurrent episodes of muscle weakness, with an incidence of 0.001%. Normokalemic periodic paralysis (NormoKPP) as the rarest subtype of PP contains both familial and sporadic. Familial NormoKPP caused by the p.M1592V mutation of the s...

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Bibliographic Details
Main Authors: Chao Fu, Zhenyu Wang, Libo Wang, Jia Li, Qiuling Sang, Jiajun Chen, Ling Qi, Hui Jin, Xiaoyang Liu
Format: Article
Language:English
Published: Frontiers Media S.A. 2018-06-01
Series:Frontiers in Neurology
Subjects:
normokalemic periodic paralysis
SCN4A
mutations
pedigree
respiratory muscle paralysis
Online Access:https://www.frontiersin.org/article/10.3389/fneur.2018.00430/full

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https://www.frontiersin.org/article/10.3389/fneur.2018.00430/full

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