Chinese patients with p.Arg756 mutations of ATP1A3: Clinical manifestations, treatment, and follow‐up

Chinese patients with p.Arg756 mutations of ATP1A3: Clinical manifestations, treatment, and follow‐up

ABSTRACT Importance The phenotypes of ATP1A3 gene mutations are diverse. Relapsing encephalopathy with cerebellar ataxia and fever‐induced paroxysmal weakness and encephalopathy (FIPWE) are considered non‐classical phenotypes caused by p.Arg756 mutations of ATP1A3. Objective To summarize the clinica...

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Bibliographic Details
Main Authors: Weihua Zhang, Jiuwei Li, Xiuwei Zhuo, Ji Zhou, Weixing Feng, Shuai Gong, Xiaotun Ren, Changhong Ding, Tongli Han, Fang Fang
Format: Article
Language:English
Published: Wiley 2022-03-01
Series:Pediatric Investigation
Subjects:
ATP1A3
Mutation
Encephalopathy
Fever
Online Access:https://doi.org/10.1002/ped4.12310

Internet

https://doi.org/10.1002/ped4.12310

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