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congenital narrowing of cervical spinal canal - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

congenital narrowing of cervical spinal canal

MONDO:0019357

Also known as:congenital stenosis of the cervical spinecongenital cervical spinal stenosis

Overview

Congenital cervical spinal stenosis is a rare neurological disease characterized by a congenital narrowing of the bony anatomy of the cervical spinal canal (sagittal diameter <14mm), predisposing the individual to symptomatic neural compression, such as cramps, paresthesias, pain, muscle hypertonia and weakness, myelopathy and sphincter disturbances.

Diagnosis

Biomarker and diagnostic research for congenital narrowing of cervical spinal canal 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 congenital narrowing of cervical spinal canal.

26 publications have been identified in PubMed for congenital narrowing of cervical spinal canal. Research spans Case Report / Case Series (31%), Diagnostic / Biomarker (27%), and Epidemiology / Natural History (15%).

Research Type	Count	% of Total
Patient case studies	8	31%

Data assembled from 3 of 12 sources · Last updated Sep 20, 2026, 9:32 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:831

GARD

Genetic and Rare Diseases Info Center

GARD:18706

Questions for Your Care Team

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congenital narrowing of cervical spinal canal

Overview

Diagnosis

Research Landscape

Medical References

External Resources

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

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