Evidence map›Paper›PMID 26598494›Full record

ReviewBrain : a journal of neurology2015

The clinical and genetic heterogeneity of paroxysmal dyskinesias.

Alice R Gardiner, Fatima Jaffer, Russell C Dale, Robyn Labrum, Roberto Erro, Esther Meyer, Georgia Xiromerisiou, Maria Stamelou, Matthew Walker, Dimitri Kullmann and 6 more

Registry-linked trialOpen access · bronzeAbstract readReview
In one paragraph

Review in Brain : a journal of neurology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04023656 (Prognosis of Paroxysmal Kinesigenic Choreoathetosis in Korea), which is not on this map. Cited by 74 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed, 1 pooled it
10.3field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT04023656 recruitingnot on this mapstarted 2016, after this paper: background citation

Prognosis of Paroxysmal Kinesigenic Choreoathetosis in Korea: a Prospective, Observational Study

Typeobservational_patient_registrySponsorSeoul National University HospitalRan2016 to 2026Enrolled100ConditionsParoxysmal Kinesigenic Choreoathetosis
3 · Its place in the literature

Who cites it

74 citing papers in PubMed, 1 synthesis or guideline pooled it, 156 citations in OpenAlex.

  1. Episodic Ataxias: Primary and Secondary Etiologies, Treatment, and Classification Approaches.Tremor and other hyperkinetic movements (New York, N.Y.) · 2023
    Pooled it
  2. Hemiplegic migraine: genetics and pathophysiology.The Journal of clinical investigation · 2026
    Review
  3. Missense Variants in the A Isoform of FGF13 as a Novel Cause of Paroxysmal Dyskinesia.Movement disorders : official journal of the Movement Disorder Society · 2026
    Article
  4. The Second Hit Hypothesis in Animal and Human Dystonia: The Role of Peripheral Nerve Trauma and Spinal Cord Injury.Movement disorders : official journal of the Movement Disorder Society · 2026
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Update on Genetic Chorea.European journal of neurology · 2025
    Review
  10. Review
  11. Paroxysmal Non-Kinesigenic Dyskinesias Associated with Biallelic POLG Variants: A Case Report.Movement disorders : official journal of the Movement Disorder Society · 2024
    Article
  12. Article
  13. Review
  14. Clinical characteristics of patients with migraine accompanied by tremor.Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2024
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

14 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 4 institutions in 4 countries.

Alice R Gardiner1 MRC Centre for Neuromuscular Diseases, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK 2 Department of Molecular Neuroscience, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK.
Fatima Jaffer1 MRC Centre for Neuromuscular Diseases, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK 2 Department of Molecular Neuroscience, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK.
Russell C Dale3 Paediatrics and Child Health, Children's Hospital, Westmead, University of Sydney, Australia.
Robyn Labrum4 Neurogenetics Laboratory, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK.
Roberto Erro5 Department of Motor Neuroscience and Movement Disorders, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK.
Esther Meyer6 Developmental Neurosciences, UCL Institute of Child Health, London WC1N 3JH, UK.
Georgia Xiromerisiou2 Department of Molecular Neuroscience, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK 7 Department of Neurology, Papageorgiou Hospital, Thessaloniki University of Athens, Greece.
Maria Stamelou5 Department of Motor Neuroscience and Movement Disorders, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK 8 Department of Neurology University of Athens, Greece 9 Department of Neurology, Philipps University, Marburg, Germany.
Matthew Walker10 Department of Experimental Epilepsy, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK.
Dimitri Kullmann10 Department of Experimental Epilepsy, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK.
Tom Warner2 Department of Molecular Neuroscience, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK.
Paul Jarman5 Department of Motor Neuroscience and Movement Disorders, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK.
Mike Hanna1 MRC Centre for Neuromuscular Diseases, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK.
Manju A Kurian6 Developmental Neurosciences, UCL Institute of Child Health, London WC1N 3JH, UK 11 Department of Neurology, Great Ormond Street Hospital, London WC1N, UK.
Kailash P Bhatia5 Department of Motor Neuroscience and Movement Disorders, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK.
Henry Houlden1 MRC Centre for Neuromuscular Diseases, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK 2 Department of Molecular Neuroscience, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK 4 Neurogenetics Laboratory, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK h.houlden@ucl.ac.uk.
University College London · GBNational Hospital for Neurology and Neurosurgery · GBNational and Kapodistrian University of Athens · GRUniversity of Sydney · AU

Funding

Medical Research Council G0200373Medical Research Council G0801316Medical Research Council G0802158Medical Research Council G0802760Medical Research Council G1001253Medical Research Council G108/638Medical Research Council G116/147Medical Research Council MR/J004758/1Medical Research Council MR/L01095X/1Wellcome Trust 104033Wellcome Trust WT093205MAWellcome Trust WT104033AIA
6 · The paper itself

Abstract

Paroxysmal dyskinesia can be subdivided into three clinical syndromes: paroxysmal kinesigenic dyskinesia or choreoathetosis, paroxysmal exercise-induced dyskinesia, and paroxysmal non-kinesigenic dyskinesia. Each subtype is associated with the known causative genes PRRT2, SLC2A1 and PNKD, respectively. Although separate screening studies have been carried out on each of the paroxysmal dyskinesia genes, to date there has been no large study across all genes in these disorders and little is known about the pathogenic mechanisms. We analysed all three genes (the whole coding regions of SLC2A1 and PRRT2 and exons one and two of PNKD) in a series of 145 families with paroxysmal dyskinesias as well as in a series of 53 patients with familial episodic ataxia and hemiplegic migraine to investigate the mutation frequency and type and the genetic and phenotypic spectrum. We examined the mRNA expression in brain regions to investigate how selective vulnerability could help explain the phenotypes and analysed the effect of mutations on patient-derived mRNA. Mutations in the PRRT2, SLC2A1 and PNKD genes were identified in 72 families in the entire study. In patients with paroxysmal movement disorders 68 families had mutations (47%) out of 145 patients. PRRT2 mutations were identified in 35% of patients, SLC2A1 mutations in 10%, PNKD in 2%. Two PRRT2 mutations were in familial hemiplegic migraine or episodic ataxia, one SLC2A1 family had episodic ataxia and one PNKD family had familial hemiplegic migraine alone. Several previously unreported mutations were identified. The phenotypes associated with PRRT2 mutations included a high frequency of migraine and hemiplegic migraine. SLC2A1 mutations were associated with variable phenotypes including paroxysmal kinesigenic dyskinesia, paroxysmal non-kinesigenic dyskinesia, episodic ataxia and myotonia and we identified a novel PNKD gene deletion in familial hemiplegic migraine. We found that some PRRT2 loss-of-function mutations cause nonsense mediated decay, except when in the last exon, whereas missense mutations do not affect mRNA. In the PNKD family with a novel deletion, mRNA was truncated losing the C-terminus of PNKD-L and still likely loss-of-function, leading to a reduction of the inhibition of exocytosis, and similar to PRRT2, an increase in vesicle release. This study highlights the frequency, novel mutations and clinical and molecular spectrum of PRRT2, SLC2A1 and PNKD mutations as well as the phenotype-genotype overlap among these paroxysmal movement disorders. The investigation of paroxysmal movement disorders should always include the analysis of all three genes, but around half of our paroxysmal series remain genetically undefined implying that additional genes are yet to be identified.

Indexed as

Genetic HeterogeneityAdolescentAdultAgedChildChoreaFemaleGlucose Transporter Type 1HumansMaleMembrane ProteinsMiddle AgedMigraine with AuraMuscle ProteinsMutationNerve Tissue ProteinsGlucose Transporter Type 1Membrane ProteinsMuscle ProteinsNerve Tissue ProteinsPNKD protein, humanPRRT2 protein, humanRNA, MessengerSLC2A1 protein, humangeneparoxysmal movement disorderPNKDPRRT2SLC2A1

Identifiers

PMID26598494
PMCPMC4655345
OpenAlexW2175680907

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.