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CAKUTCongenital Anomalies of the Kidney and Urinary Tract
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from our neighboring country in which study they also excluded the CAKUT.
High frequency of kidney and urinary tract anomalies in asymptomatic first-degree relatives of patients with CAKUT.
Early diagnosis and appropriate management can prevent development of complications in many infants with CAKUT.
Oligohydramnios is most commonly the consequence of CAKUT.
One of the most common mutated genes in CAKUT is PAX2, a gene that serves a central role in renal development.
Of importance is the history of the antenatal period with regard to CAKUT in the fetus, including oligohydramnios, maternal disease (e.
There is no association between spontaneous pneumothorax in a newborn and CAKUT