Zerres K, Mücher G, Becker J, Steinkamm C, Rudnik-Schöneborn S, Heikkilä P, Rapola J, Salonen R, Germino GG, Onuchic L, Somlo S, Avner ED, Harman LA, Stockwin JM, Guay-Woodford LM. Prenatal diagnosis of autosomal recessive polycystic kidney disease (ARPKD): molecular genetics, clinical experience, and fetal morphology. Am J Med Genet. 1998;76:137–44.

Article  CAS  PubMed  Google Scholar 

Liebau MC. Early clinical management of autosomal recessive polycystic kidney disease. Pediatr Nephrol. 2021;36:3561–70.

Article  PubMed  PubMed Central  Google Scholar 

Sweeney WE Jr, Avner ED. Diagnosis and management of childhood polycystic kidney disease. Pediatr Nephrol. 2011;26:675–92.

Article  PubMed  Google Scholar 

Guay-Woodford LM, Desmond RA. Autosomal recessive polycystic kidney disease: the clinical experience in North America. Pediatrics. 2003;111(5 Pt 1):1072–80.

Article  PubMed  Google Scholar 

Nishi K, Kamei K, Ogura M, Sato M, Ishiwa S, Shioda Y, Kiyotani C, Matsumoto K, Nozu K, Ishikura K, Ito S. Risk factors for post-nephrectomy hypotension in pediatric patients. Pediatr Nephrol. 2021;36:3699–709.

Article  PubMed  Google Scholar 

van Lieburg AF, Monnens LA. Persistent arterial hypotension after bilateral nephrectomy in a 4-month-old infant. Pediatr Nephrol. 2001;16:604–5.

Article  PubMed  Google Scholar 

Burgmaier K, Ariceta G, Bald M, Buescher AK, Burgmaier M, Erger F, Gessner M, Gokce I, Konig J, Kowalewska C, Massella L, Mastrangelo A, Mekahli D, Pape L, Patzer L, Potemkina A, Schalk G, Schild R, Shroff R, Szczepanska M, Taranta-Janusz K, Tkaczyk M, Weber LT, Wühl E, Wurm D, Wygoda S, Zagozdzon I, Dötsch J, Oh J, Schaefer F, Liebau MC, ARegPKD Consortium. Severe neurological outcomes after very early bilateral nephrectomies in patients with autosomal recessive polycystic kidney disease (ARPKD). Sci Rep. 2020;10:16025.

Article  CAS  PubMed  PubMed Central  Google Scholar 

Sweeney WE, Gunay-Aygun M, Patil A, Avner ED. Childhood polycystic kidney disease. In: Avner ED, Harmon WE, Niaudet P, editors. Pediatric nephrology. 7th ed. Berlin: Springer; 2016. p. 1103–53.

Chapter  Google Scholar 

Cole BR, Conley SB, Stapleton FB. Polycystic kidney disease in the first year of life. J Pediatr. 1987;111:693–9.

Article  CAS  PubMed  Google Scholar 

Imani PD, Carpenter JL, Bell CS, Brandt ML, Braun MC, Swartz SJ. Peritoneal dialysis catheter outcomes in infants initiating peritoneal dialysis for end-stage renal disease. BMC Nephrol. 2018;19:231.

Article  PubMed  PubMed Central  Google Scholar 

Gautam SC, Lim J, Jaar BG. Complications associated with continuous RRT. Kidney360. 2022;3:1980–90.

Article  PubMed  PubMed Central  Google Scholar 

Vidal E, Parolin M, Gamba P. Unilateral or bilateral early nephrectomy in infants with autosomal recessive polycystic kidney disease? Weighing risks and benefits. J Pediatr Surg. 2021;56:435–6.

Article  PubMed  Google Scholar 

Overman RE, Criss CN, Modi ZJ, Gadepalli SK. Early nephrectomy in neonates with symptomatic autosomal recessive polycystic kidney disease. J Pediatr Surg. 2021;56:328–31.

Article  PubMed  Google Scholar 

Mallett TM, O’Hagan E, McKeever KG. Early bilateral nephrectomy in infantile autosomal recessive polycystic kidney disease. BMJ Case Rep. 2015. https://doi.org/10.1136/bcr-2015-211106.

Article  PubMed  PubMed Central  Google Scholar 

Shukla AR, Kiddoo DA, Canning DA. Unilateral nephrectomy as palliative therapy in an infant with autosomal recessive polycystic kidney disease. J Urol. 2004;172(5 Pt 1):2000–1.

Article  PubMed  Google Scholar 

Abdul Majeed N, Font-Montgomery E, Lukose L, Bryant J, Veppumthara P, Choyke PL, Turkbey IB, Heller T, Gahl WA, Gunay-Aygun M. Prospective evaluation of kidney and liver disease in autosomal recessive polycystic kidney disease-congenital hepatic fibrosis. Mol Genet Metab. 2020;131:267–76.

Article  CAS  PubMed  Google Scholar 

Rossetti S, Harris PC. Genotype-phenotype correlations in autosomal dominant and autosomal recessive polycystic kidney disease. J Am Soc Nephrol. 2007;18:1374–80.

Article  CAS  PubMed  Google Scholar 

Burgmaier K, Brinker L, Erger F, Beck BB, Benz MR, Bergmann C, Boyer O, Collard L, Dafinger C, Fila M, Kowalewska C, Lange-Sperandio B, Massella L, Mastrangelo A, Mekahli D, Miklaszewska M, Ortiz-Bruechle N, Patzer L, Prikhodina L, Ranchin B, Ranguelov N, Schild R, Seeman T, Sever L, Sikora P, Szczepanska M, Teixeira A, Thumfart J, Uetz B, Weber LT, Wühl E, Zerres K, Dötsch J, Schaefer F, Liebau MC. Refining genotype-phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variants. Kidney int. 2021;100:650–9.

Article  CAS  PubMed  Google Scholar 

Akarkach A, Burgmaier K, Sander A, Hooman N, Sever L, Cano F, Zambrano P, Bilge I, Flynn JT, Yavascan O, Vallés PG, Munarriz RL, Patel HP, Serdaroglu E, Koch VH, Suarez ADC, Galanti M, Celedon CG, Rébori A, Kari JA, Wong CJ, Elenberg E, Rojas LF, Warady BA, Liebau MC, Schaefer F, IPPN Registry. Maintenance peritoneal dialysis in children with autosomal recessive polycystic kidney disease: a comparative cohort study of the international pediatric peritoneal dialysis network registry. Am J Kidney Dis. 2020;75:460–4.

Article  PubMed  Google Scholar