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Article

PRRT2 Mutation and Serum Cytokines in Paroxysmal Kinesigenic Dyskinesia.

Current medical science - 1 Apr 2022

Xu Ke, Huang Shan-Shan, Yue Dao-Yuan, Li Guo, Zhu Sui-Qiang, Liu Xiao-Yan

Abstract excerpt

OBJECTIVE: Paroxysmal kinesigenic dyskinesia (PKD) is a rare movement disorder PRRT2 gene mutations have been reported to cause PKD. However, the pathophysiological mechanism of PKD remains unclear, and it is unknown whether an inflammatory response is involved in the occurrence of this disease. We aimed to investigate the symptomatology, genotype, and serum cytokines of patients with PKD. METHODS: We recruited...

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PMID: 35438471
DOI: 10.1007/s11596-022-2583-7

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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