FREQUENCY AND CHARACTER OF COMBINED CONGENITAL ANOMALY OF KIDNEYS AND URINARY TRACT IN STRUCTURE CAKUT-SYNDROME IN CHILDREN
https://doi.org/10.24884/1561-6274-2018-22-3-51-57
Abstract
THE AIM. Identify the frequency and nature of the combined congenital anomaly of kidney and urinary tract development in the structure of isolated and syndromic CAKUT syndrome in 100 children. PATIENTS AND METHODS. 100 children (57 boys and 43 girls) with CAKUT syndrome, aged 2 months to 17 years, were examined. RESULTS. Out of 100 patients, 94% were isolated and 6% had syndrome CAKUT syndrome. Stratification of stage of CKD C1–5 was performed taking into account the glomerular filtration rate in 85 children with CAKUT (aged 2–17 years), the predominance С1 (74%).
About the Authors
I. Kutyrlo
Saint-Petersburg Pediatric State Medical University
Russian Federation
Russian Federation
N. Savenkova
Saint-Petersburg Pediatric State Medical University
Russian Federation
Russian Federation
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Review
For citations:
Kutyrlo I., Savenkova N. FREQUENCY AND CHARACTER OF COMBINED CONGENITAL ANOMALY OF KIDNEYS AND URINARY TRACT IN STRUCTURE CAKUT-SYNDROME IN CHILDREN. Nephrology (Saint-Petersburg). 2018;22(3):51-57. (In Russ.) https://doi.org/10.24884/1561-6274-2018-22-3-51-57
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