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longitudinal vaginal septum - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

longitudinal vaginal septum

MONDO:0015849

Overview

A rare vaginal malformation characterized by the presence of a complete or incomplete septum dividing the vagina into two parallel cavities, resulting from failure of reabsorption of the midline uterine septum between the two fused Müllerian ducts during embryogenesis. Patients are often asymptomatic, but may present with menorrhagia, dysmenorrhea, dyspareunia, infertility, or spontaneous abortion. The condition may occur as an isolated malformation or in association with other Müllerian duct anomalies (such as septate uterus or uterus didelphys) or renal abnormalities.

Diagnosis

Biomarker and diagnostic research for longitudinal vaginal septum 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 longitudinal vaginal septum.

30 publications have been identified in PubMed for longitudinal vaginal septum. Research spans Case Report / Case Series (50%), Epidemiology / Natural History (17%), and Review / Meta-Analysis (10%).

Research Type	Count	% of Total
Patient case studies	15	50%

Data assembled from 3 of 12 sources · Last updated Sep 20, 2026, 1:00 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:180157

GARD

Genetic and Rare Diseases Info Center

GARD:20190

Questions for Your Care Team

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longitudinal vaginal septum

Overview

Diagnosis

Research Landscape

Medical References

External Resources

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

Recent Publications