# Congenital Varicella Syndrome and Crossed Nonfused Renal Ectopia in a Neonate: A Case Report

**Authors:** Neha Jain, Vivek Goyal, Sreevidya Sreekantha

PMC · DOI: 10.7759/cureus.94368 · Cureus · 2025-10-11

## TL;DR

A newborn with congenital varicella syndrome also had a rare kidney anomaly, but the two conditions were likely unrelated.

## Contribution

This case report documents a rare co-occurrence of congenital varicella syndrome and crossed nonfused renal ectopia in a neonate.

## Key findings

- The neonate exhibited typical signs of congenital varicella syndrome, including skin lesions and neurological issues.
- Radiological imaging confirmed the presence of crossed nonfused renal ectopia, a rare renal anomaly.
- Maternal and neonatal varicella IgG serology confirmed the infection, but no direct link between the infection and the renal anomaly was established.

## Abstract

Congenital varicella syndrome (CVS) is a rare consequence of maternal varicella infection during early pregnancy and is characterized by cicatricial skin lesions, neurological impairment, limb hypoplasia, and ocular abnormalities. Renal anomalies are not classical features but may occur. We report a term male neonate, born to a primigravida mother with a history of varicella infection at 12 weeks of gestation. The neonate presented with perinatal asphyxia, seizures, cicatricial skin lesions, and a rare renal anomaly - crossed nonfused renal ectopia (CNRE). The neonate required resuscitation at birth, developed hypoxic-ischemic encephalopathy, and was managed with therapeutic hypothermia and antiepileptics. Radiological imaging revealed CNRE. Both maternal and neonatal varicella IgG serology were positive. The baby improved with supportive management and was discharged in stable condition. To the best of our knowledge, CVS and CNRE are not correlated and represent coincidental, unrelated findings in our case.

## Linked entities

- **Diseases:** Congenital varicella syndrome (MONDO:0017372), perinatal asphyxia (MONDO:0006663), hypoxic-ischemic encephalopathy (MONDO:0006663)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Diseases:** Renal Ectopia (MESH:C563268), CNRE (MESH:D000069337), neurological impairment (MESH:D009422), ocular abnormalities (MESH:D005124), ischemic encephalopathy (MESH:D002545), hypoxic (MESH:D002534), Renal anomalies (MESH:C535986), limb hypoplasia (MESH:C566308), asphyxia (MESH:D001237), seizures (MESH:D012640), varicella (MESH:D002644), hypothermia (MESH:D007035), CVS (MESH:D000073618), cicatricial skin lesions (MESH:D012871)

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12605621/full.md

## References

15 references — full list in the complete paper: https://tomesphere.com/paper/PMC12605621/full.md

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Source: https://tomesphere.com/paper/PMC12605621