Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

A Premature Baby with Severe Oligohydramnios and Hypotension: a Case Report of Renal Tubular Dysgenesis.

Journal of Korean medical science - 17 Aug 2020

Min Jeesu, Cho Myung Hyun, Bae Seong Phil, Shin Seung Han, Ha Il Soo, Cheong Hae Il, Kang Hee Gyung

Abstract excerpt

Renal tubular dysgenesis (RTD) is a rare fatal disorder in which there is poor development of proximal tubules, leading to oligohydramnios and the Potter sequences. RTD occurs secondary to renin-angiotensin system (RAS) blockade during the early stages of fetal development or due to autosomal recessive mutation of genes in the RAS pathway. A boy born at 33+1 weeks due to cord prolapse was found to be anuric and...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Hypotension
Share to Heart Rate

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Infant, Premature

Share to Kidney Tubules, Proximal

Share to Peptidyl-Dipeptidase A

Share to Pregnancy Complications

Share to Ultrasonography

Share to Urogenital Abnormalities

Source

Open in PubMed Open full text

Identifiers

PMID: 32808512
DOI: 10.3346/jkms.2020.35.e283
PMCID: PMC7431287

Genes

ACE

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A Premature Baby with Severe Oligohydramnios and Hypotension: a Case Report of Renal Tubular Dysgenesis.PMID 32808512Read ↗

[RENAL TUBULAR DYSGENESIS SECONDARY TO MUTATIONS IN GENES ENCODING THE RENIN-ANGIOTENSIN SYSTEM].Semantic proximity Read ↗

Spectrum of mutations in the renin-angiotensin system genes in autosomal recessive renal tubular dysgenesis.Semantic proximity Read ↗

A novel homozygous variant in REN in a family presenting with classic features of disorders involving the renin-angiotensin pathway, without renal tubular dysgenesis.Semantic proximity Read ↗

[Mutations in renin-angiotensin system genes and kidney developmental anomalies].Semantic proximity Read ↗

Renin-angiotensin system in kidney development: renal tubular dysgenesis.Semantic proximity Read ↗

Renal tubular dysgenesis and microcolon, a novel association. Report of three cases.Semantic proximity Read ↗

Congenital anomalies of the kidney and urinary tract: An embryogenetic reviewSemantic proximity Read ↗

Mutations in genes in the renin-angiotensin system are associated with autosomal recessive renal tubular dysgenesis.Semantic proximity Read ↗

Inherited renal tubular dysgenesis may not be universally fatal.Semantic proximity Read ↗

[Renal tubular dysgenesis and mutation in the renin gene].Semantic proximity Read ↗

[Renal tubular dysgenesis and mutations in the renin-angiotensin system genes].Semantic proximity Read ↗

A Primer on Congenital Anomalies of the Kidneys and Urinary Tracts (CAKUT).Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.