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kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome

MONDO:0044648

Also known as:kyphoscoliosis-lateral tongue atrophy-HSP syndrome

Overview

Diagnosis

Biomarker and diagnostic research for kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome has been reported in the published literature.

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.

No clinical trials have been registered for kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome.

101 publications have been identified in PubMed for kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome. Kisho has analyzed 32 by research type. Research spans Review / Meta-Analysis (41%), Case Report / Case Series (16%), and Diagnostic / Biomarker (13%).

Research Type	Count	% of Total
Research summaries	13

Data assembled from 3 of 12 sources · Last updated Sep 20, 2026, 11:37 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:496689

GARD

Genetic and Rare Diseases Info Center

GARD:22012

Questions for Your Care Team

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kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome

Overview

Diagnosis

Prognosis

Research Landscape

Medical References

External Resources

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

Recent Publications