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striatonigral degeneration - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

striatonigral degeneration

MONDO:0003122

Overview

A progressive neurodegenerative disorder caused by a disruption in the connection between the striatum and the substantia nigra. It is a type of multiple system atrophy (MSA). Signs and symptoms include rigidity, instability, impaired speech, and slow movements.

ResearchLimited published research (9 articles)

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.

No clinical trials have been registered for striatonigral degeneration.

10 publications have been identified in PubMed for striatonigral degeneration. Research spans Review / Meta-Analysis (33%), Case Report / Case Series (22%), and Other (11%).

Recent Publications

Gebre RK (2026). [PMID: 41912595](https://pubmed.ncbi.nlm.nih.gov/41912595/). *Sci Rep*. [Epidemiology / Natural History]
Xiao S (2026). [PMID: 41738058](https://pubmed.ncbi.nlm.nih.gov/41738058/). *Neuropsychiatr Dis Treat*. [Review / Meta-Analysis]
Lindsay R (2026). [PMID: 40888261](https://pubmed.ncbi.nlm.nih.gov/40888261/). *Mov Disord Clin Pract*. [Case Report / Case Series]
Garg S (2026). [PMID: 41232996](https://pubmed.ncbi.nlm.nih.gov/41232996/). *Neurol Clin*. [Review / Meta-Analysis]
Cuinat S (2025). [PMID: 40443206](https://pubmed.ncbi.nlm.nih.gov/40443206/). *Mov Disord Clin Pract*. [Other]
Calakos N (2025). [PMID: 39467044](https://pubmed.ncbi.nlm.nih.gov/39467044/). *Mov Disord*. [Review / Meta-Analysis]

Data assembled from 2 of 12 sources · Last updated Sep 19, 2026, 6:44 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

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striatonigral degeneration

Overview

Research Landscape

Recent Publications

Medical References

Subtypes

Related Diseases

Questions for Your Care Team

Questions for Your Care Team