# Transient Congenital Nephrotic Syndrome in Neonates: Two Case Reports and Review of Recent Literature

**Authors:** Tahani Almohayya, Abdulrahman A Al Zahrani, Samya M Edris, Hammad Alshaya

PMC · DOI: 10.7759/cureus.94722 · Cureus · 2025-10-16

## TL;DR

Two neonates with non-genetic transient congenital nephrotic syndrome showed spontaneous recovery, highlighting uncertainties in diagnosis and suggesting a possible redefinition of the condition.

## Contribution

The study presents two novel cases of transient congenital nephrotic syndrome without genetic or infectious causes, suggesting a possible stress-induced phenotype.

## Key findings

- Both neonates presented with hydrops fetalis, nephrotic range proteinuria, and hypoalbuminemia but no genetic or infectious cause was identified.
- Supportive therapy led to spontaneous recovery within weeks, with resolution of proteinuria and normalization of serum albumin.
- The cases suggest a possible transient or stress-induced phenotype of congenital nephrotic syndrome not previously well-characterized.

## Abstract

We report two cases of non-genetic transient congenital nephrotic syndrome (CNS) in neonates, both presenting with hydrops fetalis associated with nephrotic range proteinuria and significant hypoalbuminemia. Investigations did not reveal any underlying genetic cause or congenital infection to explain the nephrotic syndrome. Both cases received supportive therapy and showed spontaneous recovery with resolution of proteinuria and normalization of serum albumin in a few weeks. These cases underscore the diagnostic and prognostic uncertainties in CNS without identifiable genetic or infectious causes and highlight a possible transient or stress-induced phenotype not previously well-characterized in the literature. Furthermore, this raises the question of whether we need to redefine the definition of CNS by adding a minimum duration after which an infant will be labeled as having CNS.

## Linked entities

- **Diseases:** congenital nephrotic syndrome (MONDO:0002350), hydrops fetalis (MONDO:0015193)

## Full-text entities

- **Genes:** ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}
- **Diseases:** hypoalbuminemia (MESH:D034141), CNS (MESH:C535761), congenital infection (MESH:D007239), nephrotic (MESH:D009404), proteinuria (MESH:D011507), hydrops fetalis (MESH:D015160)

## Full text

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## Figures

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## References

14 references — full list in the complete paper: https://tomesphere.com/paper/PMC12619633/full.md

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Source: https://tomesphere.com/paper/PMC12619633