Congenital anomalies of the kidney and urinary tract (CAKUT) are the commonest cause of
chronic kidney disease in children. Structural anomalies within the CAKUT spectrum include …

Background In recent years, several studies have been published on the prognosis of
children with congenital solitary kidney (CSK), with controversial results, and a worldwide …

Congenital anomalies of the kidneys or lower urinary tract (CAKUT) are the most common
causes of renal failure in children and account for 25% of end-stage renal disease in adults …

Purpose: To investigate the utility of whole-exome sequencing (WES) to define a molecular
diagnosis for patients clinically diagnosed with congenital anomalies of kidney and urinary …

Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary
cystic kidney disease, with patients often having a positive family history that is characterized …

Children with a solitary functioning kidney (SFK) have an increased risk of kidney injury. The
exact risk of and risk factors for kidney injury remain unknown, which impedes personalized …

Objectives There is a lack of a standardised protocol for the investigation and non-operative
management of paediatric multicystic dysplastic kidney (MCDK). Institutional protocols for …

Background: To assess multicystic dysplastic kidneys (MCDK) in children, their
complications and associated congenital genitourinary anomalies. Methods: Children with …

Purpose: We assessed renal function outcome in children with congenital solitary kidney
and evaluated prognostic risk factors. Materials and Methods: We retrospectively studied the …

Objective To determine the clinical features, long-term outcomes, and additional urological
anomalies of patients treated for multicystic dysplastic kidney (MDK). Materials and methods …