TURKISH JOURNAL OF MEDICAL SCIENCES, vol.51, no.2, pp.772-777, 2021 (SCI-Expanded)
Background/aim: In children with autosomal dominant polycystic kidney disease (ADPKD), clinical manifestations range from severe neonatal presentation to renal cysts found by chance. We aimed to evaluate demographic, clinical, laboratory findings, and genetic analysis of children with ADPKD.