Volume 23: Issue 1 (May 2024): Pediatric Kidney Disease

Murugapoopathy V, Gupta IR: A primer on congenital anomalies of the kidneys and urinary tracts (CAKUT). Clin J Am Soc Nephrol 15: 723–731, 2020 PubMed

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Murugapoopathy V, Gupta IR: A primer on congenital anomalies of the kidneys and urinary tracts (CAKUT). Clin J Am Soc Nephrol 15: 723–731, 2020 PubMed)| false
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Stonebrook E, Hoff M, Spencer JD: Congenital anomalies of the kidney and urinary tract: A clinical review. Curr Treat Options Pediatr 5: 223–235, 2019 PubMed

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Stonebrook E, Hoff M, Spencer JD: Congenital anomalies of the kidney and urinary tract: A clinical review. Curr Treat Options Pediatr 5: 223–235, 2019 PubMed)| false
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Raina R, Chakraborty R, Sethi SK, Kumar D, Gibson K, Bergmann C: Diagnosis and management of renal cystic disease of the newborn: Core curriculum 2021. Am J Kidney Dis 78: 125–141, 2021 PubMed

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Hamilton AJ, Braddon F, Casula A, Lewis M, Mallett T, Marks SD, et al.: UK Renal Registry 19th annual report: Chapter 4 Demography of the UK paediatric renal replacement therapy population in 2015. Nephron 137[Suppl 1]: 103–116, 2017 PubMed

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Hamilton AJ, Braddon F, Casula A, Lewis M, Mallett T, Marks SD, : UK Renal Registry 19th annual report: Chapter 4 Demography of the UK paediatric renal replacement therapy population in 2015. Nephron 137[Suppl 1]: 103–116, 2017 PubMed)| false
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Martz K, Stablein D: North American Pediatric Renal Trials and Collaborative Studies (NAPRTCS), 2008. Available at: https://naprtcs.org/system/files/2008_Annual_CKD_Report.pdf. Accessed February 26, 2024

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Martz K, Stablein D: North American Pediatric Renal Trials and Collaborative Studies (NAPRTCS), 2008. Available at: https://naprtcs.org/system/files/2008_Annual_CKD_Report.pdf. Accessed February 26, 2024)| false
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UK Kidney Association: UK Renal Registry 25th Annual Report, 2023. Available at: https://ukkidney.org/audit-research/annual-report. Accessed February 26, 2024

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UK Kidney Association: UK Renal Registry 25th Annual Report, 2023. Available at: https://ukkidney.org/audit-research/annual-report. Accessed February 26, 2024)| false
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Harada R, Hamasaki Y, Okuda Y, Hamada R, Ishikura K: Epidemiology of pediatric chronic kidney disease/kidney failure: Learning from registries and cohort studies. Pediatr Nephrol 37: 1215–1229, 2022 PubMed

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Harada R, Hamasaki Y, Okuda Y, Hamada R, Ishikura K: Epidemiology of pediatric chronic kidney disease/kidney failure: Learning from registries and cohort studies. Pediatr Nephrol 37: 1215–1229, 2022 PubMed)| false
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Harambat J, Bonthuis M, Groothoff JW, Schaefer F, Tizard EJ, Verrina E, et al.: Lessons learned from the ESPN/ERA-EDTA Registry. Pediatr Nephrol 31: 2055–2064, 2016 PubMed

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Harambat J, Bonthuis M, Groothoff JW, Schaefer F, Tizard EJ, Verrina E, : Lessons learned from the ESPN/ERA-EDTA Registry. Pediatr Nephrol 31: 2055–2064, 2016 PubMed)| false
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Knoers NVAM: The term CAKUT has outlived its usefulness: The case for the defense. Pediatr Nephrol 37: 2793–2798, 2022 PubMed

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Subcommittee on Urinary Tract Infection: Reaffirmation of AAP clinical practice guideline: The diagnosis and management of the initial urinary tract infection in febrile infants and young children 2–24 months of age. Pediatrics 138: e20163026, 2016 PubMed

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Talati AN, Webster CM, Vora NL: Prenatal genetic considerations of congenital anomalies of the kidney and urinary tract (CAKUT). Prenat Diagn 39: 679–692, 2019 PubMed

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Talati AN, Webster CM, Vora NL: Prenatal genetic considerations of congenital anomalies of the kidney and urinary tract (CAKUT). Prenat Diagn 39: 679–692, 2019 PubMed)| false
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Deshpande C, Hennekam RCM: Genetic syndromes and prenatally detected renal anomalies. Semin Fetal Neonatal Med 13: 171–180, 2008 PubMed

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Bonsib SM: Renal hypoplasia, from grossly insufficient to not quite enough: Consideration for expanded concepts based upon the author’s perspective with historical review. Adv Anat Pathol 27: 311–330, 2020 PubMed

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Gaffar S, Arora P, Ramanathan R: Late preterm infant with postnatal diagnosis of renal tubular dysgenesis. J Investig Med High Impact Case Rep 10:10.1177/23247096221111775, 2022 PubMed

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Yener S, Pehlivanoğlu C, Akis Yıldız Z, Ilce HT, Ilce Z: Duplex kidney anomalies and associated pathologies in children: A single-center retrospective review. Cureus 14: e25777, 2022 PubMed

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Decter RM: Renal duplication and fusion anomalies. Pediatr Clin North Am 44: 1323–1341, 1997 PubMed

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Whitten SM, Wilcox DT: Duplex systems. Prenat Diagn 21: 952–957, 2001

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Anand S, Lotfollahzadeh S: Bladder exstrophy, 2023. Available at: https://www.ncbi.nlm.nih.gov/books/NBK563156/. Accessed February 26, 2024

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Taghavi K, Sharpe C, Stringer MD: Fetal megacystis: A systematic review. J Pediatr Urol 13: 7–15, 2017 PubMed

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Rodriguez MM: Congenital anomalies of the kidney and the urinary tract (CAKUT). Fetal Pediatr Pathol 33: 293–320, 2014 PubMed

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Sananes N, Cruz-Martinez R, Favre R, Ordorica-Flores R, Moog R, Zaloszy A, et al.: Two-year outcomes after diagnostic and therapeutic fetal cystoscopy for lower urinary tract obstruction. Prenat Diagn 36: 297–303, 2016 PubMed

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Sananes N, Cruz-Martinez R, Favre R, Ordorica-Flores R, Moog R, Zaloszy A, : Two-year outcomes after diagnostic and therapeutic fetal cystoscopy for lower urinary tract obstruction. Prenat Diagn 36: 297–303, 2016 PubMed)| false
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Cordido A, Vizoso-Gonzalez M, Garcia-Gonzalez MA: Molecular pathophysiology of autosomal recessive polycystic kidney disease. Int J Mol Sci 22: 6523, 2021 PubMed

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Raina R, Houry A, Rath P, Mangat G, Pandher D, Islam M, et al.: Clinical utility and tolerability of tolvaptan in the treatment of autosomal dominant polycystic kidney disease (ADPKD). Drug Healthc Patient Saf 14: 147–159, 2022 PubMed

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Raina R, Houry A, Rath P, Mangat G, Pandher D, Islam M, : Clinical utility and tolerability of tolvaptan in the treatment of autosomal dominant polycystic kidney disease (ADPKD). Drug Healthc Patient Saf 14: 147–159, 2022 PubMed)| false
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Krishnappa V, Vinod P, Deverakonda D, Raina R: Autosomal dominant polycystic kidney disease and the heart and brain. Cleve Clin J Med 84: 471–481, 2017 PubMed

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Krishnappa V, Vinod P, Deverakonda D, Raina R: Autosomal dominant polycystic kidney disease and the heart and brain. Cleve Clin J Med 84: 471–481, 2017 PubMed)| false
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Walker EYX, Marlais M: Should we screen for intracranial aneurysms in children with autosomal dominant polycystic kidney disease? Pediatr Nephrol 38: 77–85, 2023 PubMed

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Pfeferman MB, Rocha DRD, Rodrigues FG, Pfeferman E, Heilberg IP: Echocardiographic abnormalities in autosomal dominant polycystic kidney disease (ADPKD) patients. J Clin Med 11: 5982, 2022 PubMed

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Mekahli D, Guay-Woodford LM, Cadnapaphornchai MA, Greenbaum LA, Litwin M, Seeman T, et al.: Tolvaptan for children and adolescents with autosomal dominant polycystic kidney disease: Randomized controlled trial. Clin J Am Soc Nephrol 18: 36–46, 2023 PubMed

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Mekahli D, Guay-Woodford LM, Cadnapaphornchai MA, Greenbaum LA, Litwin M, Seeman T, : Tolvaptan for children and adolescents with autosomal dominant polycystic kidney disease: Randomized controlled trial. Clin J Am Soc Nephrol 18: 36–46, 2023 PubMed)| false
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Gimpel C, Bergmann C, Bockenhauer D, Breysem L, Cadnapaphornchai MA, Cetiner M, et al.: International consensus statement on the diagnosis and management of autosomal dominant polycystic kidney disease in children and young people. Nat Rev Nephrol 15: 713–726, 2019 PubMed

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Gimpel C, Bergmann C, Bockenhauer D, Breysem L, Cadnapaphornchai MA, Cetiner M, : International consensus statement on the diagnosis and management of autosomal dominant polycystic kidney disease in children and young people. Nat Rev Nephrol 15: 713–726, 2019 PubMed)| false
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Gitomer BY, Wang W, George D, Coleman E, Nowak KL, Struemph T, et al.: Statin therapy in patients with early-stage autosomal dominant polycystic kidney disease: Design and baseline characteristics. Contemp Clin Trials 137: 107423, 2023

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Nishimura H, Yerkes E, Hohenfellner K, Miyazaki Y, Ma J, Hunley TE, et al.: Role of the angiotensin type 2 receptor gene in congenital anomalies of the kidney and urinary tract, CAKUT, of mice and men. Mol Cell 3: 1–10, 1999 PubMed

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Oshima K, Miyazaki Y, Brock JW 3rd, Adams MC, Ichikawa I, Pope JC 4th: Angiotensin type II receptor expression and ureteral budding. J Urol 166: 1848–1852, 2001 PubMed

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Ichikawa I, Kuwayama F, Pope JC 4th, Stephens FD, Miyazaki Y: Paradigm shift from classic anatomic theories to contemporary cell biological views of CAKUT. Kidney Int 61: 889–898, 2002 PubMed

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Woolf AS: The term CAKUT has outlived its usefulness: The case for the prosecution. Pediatr Nephrol 37: 2785–2791, 2022 PubMed

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Hiraoka M, Taniguchi T, Nakai H, Kino M, Okada Y, Tanizawa A, et al.: No evidence for AT2R gene derangement in human urinary tract anomalies. Kidney Int 59: 1244–1249, 2001 PubMed

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Nicolaou N, Renkema KY, Bongers EMHF, Giles RH, Knoers NVAM: Genetic, environmental, and epigenetic factors involved in CAKUT. Nat Rev Nephrol 11: 720–731, 2015 PubMed

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Dart AB, Ruth CA, Sellers EA, Au W, Dean HJ: Maternal diabetes mellitus and congenital anomalies of the kidney and urinary tract (CAKUT) in the child. Am J Kidney Dis 65: 684–691, 2015 PubMed

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Groen In ’t Woud S, Roeleveld N, van Rooij IALM, Feitz WFJ, Schreuder MF, van der Zanden LFM; SOFIA study group: Environmental and parental risk factors for congenital solitary functioning kidney - A case-control study. Pediatr Nephrol 38: 2631–2641, 2023 PubMed

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van der Ven AT, Connaughton DM, Ityel H, Mann N, Nakayama M, Chen J, et al.: Whole-exome sequencing identifies causative mutations in families with congenital anomalies of the kidney and urinary tract. J Am Soc Nephrol 29: 2348–2361, 2018 PubMed

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Kerecuk L, Sajoo A, McGregor L, Berg J, Haq MR, Sebire NJ, et al.: Autosomal dominant inheritance of non-syndromic renal hypoplasia and dysplasia: dramatic variation in clinical severity in a single kindred. Nephrol Dial Transplant 22: 259–263, 2007 PubMed

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Sanna-Cherchi S, Ravani P, Corbani V, Parodi S, Haupt R, Piaggio G, et al.: Renal outcome in patients with congenital anomalies of the kidney and urinary tract. Kidney Int 76: 528–533, 2009 PubMed

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Wühl E, van Stralen KJ, Verrina E, Bjerre A, Wanner C, Heaf JG, et al.: Timing and outcome of renal replacement therapy in patients with congenital malformations of the kidney and urinary tract. Clin J Am Soc Nephrol 8: 67–74, 2013 PubMed

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Ritchie AG, Clayton PA, Mackie FE, Kennedy SE: Nationwide survey of adolescents and young adults with end-stage kidney disease. Nephrology (Carlton) 17: 539–544, 2012 PubMed

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Forbes TA, Watson AR, Zurowska A, Shroff R, Bakkaloglu S, Vondrak K, et al.; European Paediatric Dialysis Working Group: Adherence to transition guidelines in European paediatric nephrology units. Pediatr Nephrol 29: 1617–1624, 2014 PubMed

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