# Obstructed Hemivagina and Ipsilateral Renal Anomaly (OHVIRA) Syndrome: A Diagnosis in the First Year of Life

**Authors:** Carolina Quintela, Ana Sofia Figueiredo, Andreia Dias, António Trindade

PMC · DOI: 10.7759/cureus.77265 · Cureus · 2025-01-11

## TL;DR

OHVIRA is a rare condition in females that can be diagnosed early, preventing complications like infertility or kidney failure.

## Contribution

This case demonstrates early diagnosis of OHVIRA in the first year of life through routine screening.

## Key findings

- A female child was diagnosed with OHVIRA during the first year of life due to prenatal detection of renal agenesis.
- Prompt postnatal imaging confirmed the associated gynecological malformation.
- Early diagnosis can prevent complications such as infertility or renal failure.

## Abstract

Obstructed hemivagina and ipsilateral renal anomaly (OHVIRA) is a rare congenital anomaly that affects females. Although it is possible to diagnose in early life, most cases are usually diagnosed in adolescence or adulthood. This delay in diagnosis can cause a variety of complications, some associated with infertility or renal failure. Here, we report the case of a female child with unilateral renal agenesis identified on the prenatal scans. Prompt postnatal imaging made it possible to diagnose the concomitant gynecological malformation during the first year of life. This report highlights the importance of an early diagnosis in such cases, which could be done through routine screening for gynecological anomalies in patients with prenatal diagnosis of renal malformations.

## Linked entities

- **Diseases:** renal failure (MONDO:0001106)

## Full-text entities

- **Diseases:** congenital anomaly (MESH:D000013), renal malformations (MESH:D006030), unilateral renal agenesis (MESH:D000075529), gynecological anomalies (MESH:D005831), infertility (MESH:D007246), renal failure (MESH:D051437), OHVIRA (MESH:D012078)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

7 references — full list in the complete paper: https://tomesphere.com/paper/PMC11808342/full.md

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Source: https://tomesphere.com/paper/PMC11808342