Congenital anomalies of the kidney and urinary tract (CAKUT) cover a wide range of
structural malformations that result from defects in the morphogenesis of the kidney and/or …

Congenital anomalies of the kidneys and urinary tract (CAKUT) comprise a large spectrum
of congenital malformations ranging from severe manifestations, such as renal agenesis, to …

Background Congenital anomalies of the kidney and urinary tract (CAKUT) are the most
prevalent cause of kidney disease in the first three decades of life. Previous gene panel …

Congenital anomalies of the kidney and urinary tract (CAKUTs) occur in 3–6 per 1000 live
births, account for the most cases of pediatric end‐stage kidney disease (ESKD), and …

Congenital anomalies of the kidney and urinary tract (CAKUT) comprise a large variety of
malformations that arise from defective kidney or urinary tract development and frequently …

Congenital anomalies of the kidney and urinary tract (CAKUT) are common birth defects and
the leading cause of end-stage renal disease in children. There is a wide spectrum of renal …

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 …

During the past decades, remarkable progress has been made in our understanding of the
molecular basis of kidney diseases, as well as in the ability to pinpoint disease-causing …

Congenital anomalies of the kidney and urinary tract (CAKUT) occur in 0.5–1/100 newborns
and as a group they represent the most frequent cause for chronic kidney failure in children …

Congenital anomalies of the kidney and urinary tract (CAKUT) refer to a spectrum of
structural renal malformations and are the leading cause of end-stage renal disease in …