A Case of Familial Paroxysmal Non-kinesigenic Dyskinesia in Mainland China: A Clinical and Genetic Investigation

Paroxysmal non-kinesigenic dyskinesia (PNKD) is an autosomal dominant condition characterized by recurring dystonia or mixed chorea and ballism caused by emotional stress, exhaustion, coffee, alcohol, menstruation, and other factors. Here, we provide a large family PNKD pedigree from mainland China, where the same c.20C4T (p.Ala7Val) mutation in exon 1 of the PNKD gene was genetically confirmed to be present in nine affected individuals. Here, we report a rarely described Asian PNKD pedigree and aim to widen the clinical and genetic spectrum of PNKD while also providing fresh diagnostic insights for this rare condition.

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Publication Details

Journal
Cureus
Published
2026-01-09
DOI
https://doi.org/10.7759/cureus.101172
Primary Topic
Genomics and Rare Diseases
Type
article
Field-Weighted Citation Impact
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article

A Case of Familial Paroxysmal Non-kinesigenic Dyskinesia in Mainland China: A Clinical and Genetic Investigation

Zhongjiao LU, gang wang, Nan Zhao, Wenhan Zhang et al.
Cureus
Genomics and Rare Diseases
article

A Case of Familial Paroxysmal Non-kinesigenic Dyskinesia in Mainland China: A Clinical and Genetic Investigation

Zhongjiao LU, gang wang, Nan Zhao, Wenhan Zhang, Li Gao, Jingwen Li, Ruichuan Xie, Kan Wang, Shuang Li
article en

Abstract

Paroxysmal non-kinesigenic dyskinesia (PNKD) is an autosomal dominant condition characterized by recurring dystonia or mixed chorea and ballism caused by emotional stress, exhaustion, coffee, alcohol, menstruation, and other factors. Here, we provide a large family PNKD pedigree from mainland China, where the same c.20C4T (p.Ala7Val) mutation in exon 1 of the PNKD gene was genetically confirmed to be present in nine affected individuals. Here, we report a rarely described Asian PNKD pedigree and aim to widen the clinical and genetic spectrum of PNKD while also providing fresh diagnostic insights for this rare condition.

CureusVol. 18(1)
Renji Hospital (CN), Sanya Central Hospital (CN), Huashan Hospital (CN)
Openalex Percentile: Top 92%
Genomics and Rare Diseases
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A Case of Familial Paroxysmal Non-kinesigenic Dyskinesia in Mainland China: A Clinical and Genetic Investigation — Zhongjiao LU, gang wang, et al. · Cureus (2026) | TGRS Research Map | TGRS