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

Rare Disease

transverse vaginal septum

MONDO:0015850

Overview

A rare vaginal malformation characterized by the presence of a complete or incomplete transverse septum at any level of the vagina (most frequently the upper or middle third), resulting from incomplete fusion between the Müllerian duct component and the urogenital sinus component of the vagina during embryogenesis. The condition is only rarely diagnosed in neonates or infants, unless it causes significant hydromucocolpos. Complete septa present with primary amenorrhea, cyclic pelvic pain, dyspareunia, or a pelvic mass consisting of accumulated menstrual blood, while incomplete septa may lead to dyspareunia and dysmenorrhea.

Diagnosis

Biomarker and diagnostic research for transverse 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 transverse vaginal septum.

24 publications have been identified in PubMed for transverse vaginal septum. Research spans Case Report / Case Series (61%), Review / Meta-Analysis (22%), and Other (9%).

Research Type	Count	% of Total
Patient case studies	14	61%

Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 2:56 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:180160

GARD

Genetic and Rare Diseases Info Center

GARD:20191

Questions for Your Care Team

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transverse vaginal septum

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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