Kisho is an information platform, not a medical provider. Nothing on this site constitutes medical advice, diagnosis, or treatment recommendations. All content is aggregated from publicly available sources (including ClinicalTrials.gov, PubMed, FDA.gov, and Orphanet) and is provided for informational purposes only. Clinical trial eligibility, treatment decisions, and any health-related actions should always be discussed with a qualified healthcare professional. Kisho does not endorse any specific therapy, organization, or clinical trial. Terms of use · Privacy policy
Maternally-inherited mitochondrial dystonia is a rare neurological mitochondrial DNA-related disorder characterized clinically by progressive pediatric-onset dystonia with variable degrees of severity.
Estimated prevalence: Unknown (Unknown prevalence).
No clinical trials have been registered for maternally-inherited mitochondrial dystonia.
4 publications have been identified in PubMed for maternally-inherited mitochondrial dystonia. Research spans Review / Meta-Analysis (50%), Case Report / Case Series (25%), and Basic Science / Preclinical (25%).
Meng Y (2025). [PMID: 39937390](https://pubmed.ncbi.nlm.nih.gov/39937390/). *J Assist Reprod Genet*. [Basic Science / Preclinical]
Magro G (2025). [PMID: 40278159](https://pubmed.ncbi.nlm.nih.gov/40278159/). *J Xenobiot*. [Review / Meta-Analysis]
Ventura I (2025). [PMID: 40597358](https://pubmed.ncbi.nlm.nih.gov/40597358/). *Orphanet J Rare Dis*. [Case Report / Case Series]
Ali L (2025). [PMID: 40787643](https://pubmed.ncbi.nlm.nih.gov/40787643/). *J Biol Methods*. [Review / Meta-Analysis]
Data assembled from 3 of 12 sources · Last updated Sep 18, 2026, 8:34 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center