Whole-exome sequencing identifies causative mutations in families with congenital anomalies of the kidney and urinary tract

AT Van Der Ven, DM Connaughton, H Ityel… - Journal of the …, 2018 - journals.lww.com
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 …

Follow-up of Acute kidney injury in Neonates during Childhood Years (FANCY): a prospective cohort study

MW Harer, CF Pope, MR Conaway, JR Charlton - Pediatric Nephrology, 2017 - Springer
Background Very low birth weight (VLBW) neonates commonly experience acute kidney
injury (AKI) in the neonatal intensive care unit (NICU). We hypothesize that VLBW neonates …

Incidence, diagnosis and treatment of children's congenital abnormalities of the kidney and urinary tract detected in ultrasound screening

B Zhang, H Wang, N Sun, LQ Jia… - Zhonghua er ke za zhi …, 2011 - europepmc.org
Objective To investigate the proportion of children with congenital abnormalities of the
kidney and urinary tract (CAKUT) among those who received screening, analyze the rate …

[HTML][HTML] Early acute kidney injury in preterm and term neonates: incidence, outcome, and associated clinical features

D Gallo, KA de Bijl-Marcus, T Alderliesten, M Lilien… - Neonatology, 2021 - karger.com
Background: Critically ill neonates are at high risk of kidney injury, mainly in the first days of
life. Acute kidney injury (AKI) may be underdiagnosed due to lack of a uniform definition. In …

Incidence and outcomes of acute kidney injury in extremely-low-birth-weight infants

CC Lee, OW Chan, MY Lai, KH Hsu, TW Wu, WH Lim… - PLoS …, 2017 - journals.plos.org
Background Acute kidney injury (AKI) is a common event in the neonatal intensive care unit
(NICU), especially in extremely-low-birth-weight (ELBW) infants. This cohort study …

The genetic basis of congenital anomalies of the kidney and urinary tract

M Kagan, O Pleniceanu, A Vivante - Pediatric Nephrology, 2022 - Springer
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 …

Molecular causes of congenital anomalies of the kidney and urinary tract (CAKUT)

S Kohl, S Habbig, LT Weber, MC Liebau - Molecular and cellular …, 2021 - Springer
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 …

Late onset neonatal acute kidney injury: results from the AWAKEN Study

JR Charlton, L Boohaker, D Askenazi, PD Brophy… - Pediatric …, 2019 - nature.com
Background Most studies of neonatal acute kidney injury (AKI) have focused on the first
week following birth. Here, we determined the outcomes and risk factors for late AKI (> 7d) …

Genetic basis of human congenital anomalies of the kidney and urinary tract

S Sanna-Cherchi, R Westland… - The Journal of …, 2018 - Am Soc Clin Investig
The clinical spectrum of congenital anomalies of the kidney and urinary tract (CAKUT)
encompasses a common birth defect in humans that has significant impact on long-term …

Congenital unilateral renal agenesis: prevalence, prenatal diagnosis, associated anomalies. Data from two birth‐defect registries

H Laurichesse Delmas, M Kohler, B Doray… - Birth defects …, 2017 - Wiley Online Library
Background The different mechanisms leading to a solitary kidney should be differentiated
because the long‐term outcome might be different. The fetal period is the best moment to …