ArticleCurrent treatment options in pediatrics2019
Congenital Anomalies of the Kidney and Urinary Tract: A Clinical Review.
Article in Current treatment options in pediatrics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.
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Who cites it
25 citing papers in PubMed, 1 synthesis or guideline pooled it, 56 citations in OpenAlex.
- A systematic review of kidney transplantation outcomes in patients with end-stage renal disease due to childhood lower urinary tract malformations.International urology and nephrology · 2024Pooled it
- Focal double-lumen ureter causing upper ureteric obstruction in a pelvic ectopic kidney: A rare case report.Urology case reports · 2026Article
- Diagnostic yield of urinary tract ultrasound in children following a first urinary tract infection: a retrospective cohort study.Pediatric radiology · 2026Article
- Urological Malformations Identify the High-Burden Phenotype Among Children Hospitalized for Presumed Urinary Tract Infection: A Retrospective Cohort.Diagnostics (Basel, Switzerland) · 2026Article
- Comparison of dynamic contrast-enhanced MRI versus MAG-3 scintigraphy for differential renal function assessment in pediatric patients.Pediatric radiology · 2026Article
- Right Iliac Ectopic Kidney With an Extrarenal Pelvis, Aberrant Upper-Pole Arterial Supply, and Multiple Renal Cysts.Cureus · 2026Article
- Congenital anomalies of the kidney and urinary tract in children treated at a tertiary hospital in Northern Tanzania: assessment of coexisting congenital anomalies.World journal of pediatric surgery · 2026Article
- Adult Diagnosis of Solitary Kidney and Renal Dysplasia in a Male Born Prematurely as a Twin: A Case Report.International journal of nephrology and renovascular disease · 2026Article
- Functional Characterization of a NovelGenes · 2025Article
- Perioperative Outcomes of Ureteroscopy in Patients with Anatomical Anomalies of the Urinary Tract and Neurogenic Bladder: A Retrospective Comparative Study.Journal of clinical medicine · 2025Article
- A Case of Horseshoe Kidney and Autosomal Dominant Polycystic Kidney Disease withJournal of clinical medicine · 2025Article
- Investigation of a targeted panel of gut microbiome-derived toxins in children with chronic kidney disease.Pediatric nephrology (Berlin, Germany) · 2025Article
- Complex Management of Bilateral Congenital Hydronephrosis in a Pediatric Patient: A Multidisciplinary Approach.Healthcare (Basel, Switzerland) · 2025Article
- Genetic etiology and pregnancy outcomes of fetal hyperechoic kidneys: a retrospective analysis.Frontiers in pediatrics · 2025Article
- Prenatal Diagnosis of Reno-Urinary Malformations in a Tertiary Center of Republic of Moldavia.Diagnostics (Basel, Switzerland) · 2024Article
- Investigating low birth weight and preterm birth as potential mediators in the relationship between prenatal infections and early child development: a linked administrative health data analysis.Journal of epidemiology and community health · 2024Article
- Genetic and Clinical Factors Influencing Congenital Anomalies of the Kidney and Urinary Tract in Children: Insights from Prenatal and Postnatal Assessments.Biomedicines · 2024Article
- A Pilot Comparative Study between Creatinine- and Cystatin-C-Based Equations to Estimate GFR and Kidney Ultrasound Percentiles in Children with Congenital Anomalies of the Kidney and Urinary Tract.Diagnostics (Basel, Switzerland) · 2024Article
- Bilateral Renal Ectopia-Prenatal Diagnosis.Diagnostics (Basel, Switzerland) · 2024Article
- Review
Corrections and comments
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Authors and funding
3 authors at 1 institution in 1 country.
Funding
Abstract
purpose of reviewThis review highlights the most common congenital anomalies of the kidney and urinary tract (CAKUT) that are encountered in pediatric practices. CAKUT are the most common cause of prenatally diagnosed developmental malformations and encompass a spectrum of disorders impacting lower urinary tract development as well as kidney development and function. In pediatric and adolescent populations, developmental abnormalities are the leading cause of end-stage kidney disease. The goal of this review is to provide pediatric providers a framework for appropriate clinical management as well as highlight when referral to subspecialty care is needed. RECENT
findingsWhile the exact etiologies of CAKUT are not completely defined, new evidence demonstrates that genetic and molecular changes impact embryonic kidney and urinary tract development. As a result, phenotypes and clinical outcomes may be affected. SUMMARY: Because pediatric providers provide front-line care to children and adolescents with developmental kidney and urinary tract anomalies, updated knowledge of CAKUT pathogenesis, embryology, clinical management, and patient outcomes is needed. This manuscript reviews CAKUT etiologies and essential diagnostic, prognostic, and management strategies.
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