Discover Community Create You

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

Genetic spectrum of CAKUT and risk factors for kidney failure: a pediatric multicenter cohort study

21 Dec 2022

Abstract excerpt

BACKGROUND: Congenital anomalies of the kidney and urinary tracts (CAKUT) are the leading cause of kidney failure in children with phenotypic and genotypic heterogeneity. Our objective was to describe the genetic spectrum and identify the risk factors for kidney failure in children with CAKUT. METHODS: Clinical and genetic data were derived from a multicenter network (Chinese Children Genetic Kidney Disease...

Read the complete abstract on PubMed

Topics

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

Share to Pediatric Urology and Nephrology Studies
Share to Renal and related cancers
Share to Renal cell carcinoma treatment

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 36549658
DOI: 10.1093/ndt/gfac338

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetic spectrum of CAKUT and risk factors for kidney failure: a pediatric multicenter cohort studyPMID 36549658Read ↗

Genetic Architecture of Childhood Kidney and Urological Diseases in ChinaSemantic proximity Read ↗

Genetic Spectrum of Congenital Anomalies of the Kidney and Urinary Tract in Chinese Newborn Genome ProjectSemantic proximity Read ↗

Exome Reanalysis Identifies Novel Candidate Genes Associated with Congenital Anomalies of the Kidney and Urinary Tract in ChinaSemantic proximity Read ↗

Deciphering the Mutation Spectrum in South Indian Children With Congenital Anomalies of the Kidney and Urinary TractSemantic proximity Read ↗

Targeted Exome Sequencing Provided Comprehensive Genetic Diagnosis of Congenital Anomalies of the Kidney and Urinary TractSemantic proximity Read ↗

CAKUT subtypes determine the rate of progression to kidney failure-an adult patient cohort study.Semantic proximity Read ↗

Genetic spectrum of renal disease for 1001 Chinese children based on a multicenter registration systemSemantic proximity Read ↗

Novel perspectives for investigating congenital anomalies of the kidney and urinary tract (CAKUT)Semantic proximity Read ↗

Clinical Integration of Genome Diagnostics for Congenital Anomalies of the Kidney and Urinary Tract.Semantic proximity Read ↗

Pathophysiology of Congenital Anomalies of the Kidney and Urinary Tract: A Comprehensive Review.Semantic proximity Read ↗

Deciphering the mutation spectrum in south Indian children with congenital anomalies of the kidney and urinary tract.Semantic proximity Read ↗

Genetics of congenital anomalies of the kidney and urinary tract.Semantic proximity Read ↗

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