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Article

Clinical and Genetic Characteristics of Paroxysmal Kinesigenic Dyskinesia: A Single-Center Study and Literature Review.

FASEB journal : official publication of the Federation of American Societies for Experimental Biology - 31 Jan 2026

Li Menghua, Tan Dandan, Zhu Yu, Xiong Ying, Zhu Min, Zhou Meihong, Hong Daojun, Qiu Yusen

Abstract excerpt

Paroxysmal kinesigenic dyskinesia (PKD) is a genetically heterogeneous movement disorder primarily associated with PRRT2 variants. Recently, TMEM151A and KCNJ10 have emerged as additional PKD-associated genes. However, genotype-phenotype correlations remain poorly defined. In this study, we retrospectively analyzed 41 PKD patients from a single center in Southeastern China. All patients underwent comprehensive...

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Source

Identifiers

PMID: 41553070
DOI: 10.1096/fj.202502596R

Genes

KCNJ10
TMEM151A
PRRT2
PNKD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

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Clinical and Genetic Characteristics of Paroxysmal Kinesigenic Dyskinesia: A Single-Center Study and Literature Review.PMID 41553070Read ↗

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