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Pediatric nephrology (Berlin, Germany)

October 5, 2026 · via Europe PMC

ACE-related renal tubular dysgenesis (RTD-ACE) in a neonate surviving beyond the early neonatal period.

Abu Hussain SF, Forbes T, Kausman JY

Journal ArticleAbstract only — full text under license

AI summary — for doctors, generated from the abstract only

A preterm infant with ACE-related renal tubular dysgenesis survived beyond the neonatal period after early peritoneal dialysis.

What was studied

A single case report of a preterm neonate with genetically confirmed ACE-related renal tubular dysgenesis managed with early PD and supportive care.

Key findings

  • The condition is usually marked by oligohydramnios, refractory hypotension and anuria with very high perinatal mortality
  • Early peritoneal dialysis and targeted support allowed survival past the neonatal period
  • Early genetic diagnosis clarified the mechanism and supported ongoing intensive care
  • Postnatal changes in urine output affected counselling and decisions about dialysis

Clinical relevance

It suggests RTD is not uniformly fatal and that decisions about offering neonatal dialysis may need to consider evolving urine output.

Who should care

Nephrology

Limitations

A single case, so it does not establish how often survival is achievable.

Consider genetic diagnosis early and avoid assuming an inevitably fatal course when counselling families.

This is an AI-generated summary of the published abstract, not a clinical recommendation. It may not reflect the full text or subsequent updates — verify against the original source before acting on it.

Abstract

Renal tubular dysgenesis (RTD) is a rare autosomal recessive disorder of renal development caused by disruption of the foetal renin-angiotensin system, most commonly due to pathogenic variants in the angiotensin-converting enzyme (ACE) gene. The condition is classically associated with antenatal oligohydramnios or anhydramnios, refractory neonatal hypotension, and anuric kidney failure, with extremely high perinatal mortality. We report a preterm neonate with genetically confirmed RTD-ACE who survived beyond the neonatal period following early initiation of peritoneal dialysis and targeted supportive management. Early genetic diagnosis clarified the underlying pathophysiology and supported sustained intensive care despite the severity of presentation. This case illustrates the evolving clinical spectrum of RTD, particularly the postnatal evolution of urine output, and demonstrates the importance of this trajectory in counselling families and guiding decisions regarding the appropriateness and potential benefit of offering neonatal dialysis.

DOI

10.1007/s00467-026-07549-3

PMID

42831903

Research metadata (titles, abstracts, authors, publication dates) is sourced from Europe PMC, which aggregates content from PubMed/MEDLINE, PubMed Central, and other providers under the U.S. National Library of Medicine (NLM/NCBI). NLM does not claim copyright on abstracts; the original journal publishers or authors may hold rights to the full articles. AI-generated summaries are derived only from the abstract, never the full text, and are always labeled as AI-generated.

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