Evidence map›Paper›PMID 24285620›Full record

SynthesisNeurology2014

Prevalence of ataxia in children: a systematic review.

Kristin E Musselman, Cristina T Stoyanov, Rhul Marasigan, Mary E Jenkins, Jürgen Konczak, Susanne M Morton, Amy J Bastian

Open access · bronzeAbstract readSystematic Review
In one paragraph

Synthesis in Neurology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 25% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

38 citing papers in PubMed, 1 synthesis or guideline pooled it, 78 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. CGG Repeat Expansion in GIPC1 is Associated with Childhood-Onset Hereditary Ataxia.Movement disorders : official journal of the Movement Disorder Society · 2026
    Article
  5. Review
  6. Phenotypic Heterogeneity in Genetic and Acquired Pediatric Cerebellar Disorders.Movement disorders : official journal of the Movement Disorder Society · 2025
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Metabolites · 2022
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
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

7 authors at 4 institutions in 2 countries.

Kristin E MusselmanFrom the Department of Neuroscience (K.E.M., A.J.B.), Johns Hopkins School of Medicine, Baltimore, MD; Kennedy Krieger Institute (K.E.M., R.M., A.J.B.), Baltimore, MD; Johns Hopkins Bloomberg School of Public Health (C.T.S.), Baltimore, MD; Department of Clinical Neurological Sciences (M.E.J.), Western University, London, Ontario, Canada; School of Kinesiology (J.K.), University of Minnesota, Minneapolis; and Department of Physical Therapy (S.M.M.), University of Delaware, Newark.
Cristina T Stoyanov
Rhul Marasigan
Mary E Jenkins
Jürgen Konczak
Susanne M Morton
Amy J Bastian
Johns Hopkins University · USUniversity of Minnesota · USKennedy Krieger Institute · USWestern University · CA

Funding

MECHANISMS AND REHABILITATION OF CEREBELLAR ATAXIAR01HD040289 · NICHD · HUGO W. MOSER RES INST KENNEDY KRIEGER · PI BASTIAN, AMY J. · 2002 to 2022
$6.2M
Taskforce on Childhood Motor DisordersU13NS061384 · NINDS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI SANGER, TERENCE D · 2007 to 2009
$197k
CIHRNICHD NIH HHS R01 HD040289NINDS NIH HHS U13 NS061384
6 · The paper itself

Abstract

objectiveTo estimate the prevalence of childhood ataxia resulting from both genetic and acquired causes.

methodsA systematic review was conducted following the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-analyses) statement. Five databases were searched for articles reporting a frequency measure (e.g., prevalence, incidence) of ataxia in children. Included articles were first grouped according to the World Health Organization (WHO) regions and subsequently classified according to etiology (genetic, acquired, or mixed). Each article was assessed for its risk of bias on the domains of sampling, measurement, and analysis. Incidence values were converted to prevalence estimates whenever possible. European prevalence estimates for different etiologies of ataxia were summed to gauge the overall prevalence of childhood ataxia.

resultsOne hundred fifteen articles were included in the review. More than 50% of the data originated from the Europe WHO region. Data from this region also showed the least susceptibility to bias. Little data were available for Africa and Southeast Asia. The prevalence of acquired ataxias was found to vary more greatly across regions than the genetic ataxias. Ataxic cerebral palsy was found to be a significant contributor to the overall prevalence of childhood ataxia across WHO regions. The prevalence of childhood ataxias in Europe was estimated to be ∼26/100,000 children and likely reflects a minimum prevalence worldwide.

conclusionsThe findings show that ataxia is a common childhood motor disorder with a higher prevalence than previously assumed. More research concerning the epidemiology, assessment, and treatment of childhood ataxia is warranted.

Indexed as

Global HealthAtaxiaChildHumansPrevalenceWorld Health Organization

Identifiers

PMID24285620
PMCPMC3873624
OpenAlexW2165096064

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.