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pure or complex hereditary spastic paraplegia - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

pure or complex hereditary spastic paraplegia

MONDO:0017913

Also known as:Pure or complex familial spastic paraplegiaPure or complicated familial spastic paraplegiaPure or complicated hereditary spastic paraplegia

Overview

Diagnosis

Biomarker and diagnostic research for pure or complex hereditary spastic paraplegia has been reported in the published literature.

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 pure or complex hereditary spastic paraplegia.

247 publications have been identified in PubMed for pure or complex hereditary spastic paraplegia. Kisho has analyzed 44 by research type. Research spans Basic Science / Preclinical (36%), Review / Meta-Analysis (20%), and Epidemiology / Natural History (20%).

Research Type	Count	% of Total
Laboratory research	16	36%

Data assembled from 3 of 12 sources · Last updated Sep 18, 2026, 10:52 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:320335

GARD

Genetic and Rare Diseases Info Center

GARD:21429

Questions for Your Care Team

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pure or complex hereditary spastic paraplegia

Overview

Diagnosis

Research Landscape

Medical References

External Resources

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

Recent Publications