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autosomal recessive ataxia due to PEX10 deficiency - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

autosomal recessive ataxia due to PEX10 deficiency

MONDO:0016614

Also known as:mild peroxismal disorder due to PEX10 deficiency

Find Clinical TrialsTrials

Overview

Clinical Trials1 registered · 1 recruiting

ResearchLimited published research (4 articles)

Prognosis

Estimated prevalence: <1 in 1,000,000 (VERY_RARE).

Research Landscape

Sourced from ClinicalTrials.gov and PubMed. Publication types are classified using NLM-curated article metadata; research type breakdowns reflect the nature of published work for this disease.

1 clinical trial registered, 1 recruiting. Interventions under study include other interventions. Research is primarily sponsored by academic and government institutions.

4 publications have been identified in PubMed for autosomal recessive ataxia due to PEX10 deficiency. Research spans Review / Meta-Analysis (25%), Case Report / Case Series (25%), and Basic Science / Preclinical (25%).

Recent Publications

Sabbagh Q (2025). [PMID: 39821477](https://pubmed.ncbi.nlm.nih.gov/39821477/). *Journal of neurology*. [Basic Science / Preclinical]
Fogel BL (2025). [PMID: 40464291](https://pubmed.ncbi.nlm.nih.gov/40464291/). *Annals of neurology*. [Review / Meta-Analysis]
Huang X (2025). [PMID: 40267090](https://pubmed.ncbi.nlm.nih.gov/40267090/). *PloS one*. [Case Report / Case Series]
Gogus B (2024). [PMID: 38587696](https://pubmed.ncbi.nlm.nih.gov/38587696/). *Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology*. [Epidemiology / Natural History]

Data assembled from 4 of 12 sources · Last updated Sep 20, 2026, 5:35 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:247815

GARD

Genetic and Rare Diseases Info Center

GARD:20666

Questions for Your Care Team

→Are any of the 1 active clinical trial a good fit for my situation?
→Are there specialists or centers of excellence for this condition in my area?
→Is there a patient registry I should consider joining?

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autosomal recessive ataxia due to PEX10 deficiency

Overview

Prognosis

Research Landscape

Recent Publications

Medical References

External Resources

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team