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由CACNA1S基因突变引起的低钾性周期性麻痹。

Hypokalemic periodic paralysis due to CACNA1S gene mutation.

作者信息

Alhasan Khalid A, Abdallah Mohammed S, Kari Jameela A, Bashiri Fahad A

机构信息

Division of Pediatric Nephrology, Pediatric Department, College of Medicine, King Khalid University Hospital, King Saud University, Riyadh, Kingdom of Saudi Arabia. E-mail:

出版信息

Neurosciences (Riyadh). 2019 Jul;24(3):225-230. doi: 10.17712/nsj.2018.3.20180005.

Abstract

Hypokalemic periodic paralysis (HypoPP) is a relatively rare but treatable disorder caused by mutations in the CACNA1S gene. HypoPP patients may experience paralytic episodes associated with hypokalemia and, infrequently, may develop late-onset proximal myopathy. The paralytic attacks are characterized by reversible flaccid paralysis and, in most cases, spare the respiratory muscles and heart. We report a case of CACNA1S periodic paralysis precipitated by vigorous exercise in a 14-year-old boy who presented with sudden-onset paralysis of both his upper and lower extremities. Laboratory evaluation revealed a markedly low serum potassium level. The patients symptoms resolved after correction of the potassium abnormality, and he was discharged with no neurological deficits. Although rare, HypoPP must be differentiated from other causes of weakness and paralysis so that proper treatment can be promptly initiated to ensure good outcomes.

摘要

低钾性周期性麻痹(HypoPP)是一种相对罕见但可治疗的疾病,由CACNA1S基因突变引起。HypoPP患者可能会经历与低钾血症相关的麻痹发作,且很少会发展为迟发性近端肌病。麻痹发作的特征是可逆性弛缓性麻痹,在大多数情况下,呼吸肌和心脏不受影响。我们报告一例14岁男孩因剧烈运动诱发的CACNA1S周期性麻痹,该男孩出现双上肢和双下肢突然麻痹。实验室检查显示血清钾水平明显降低。纠正钾异常后患者症状缓解,出院时无神经功能缺损。尽管罕见,但必须将HypoPP与其他导致无力和麻痹的原因区分开来,以便能及时开始适当治疗以确保良好预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76e0/8015512/283c15182d9f/Neurosciences-24-225-g001.jpg

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