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Follow-up of children and adolescents with congenital anomalies of the kidneys and urinary tract, associated with rare hereditary syndromes
https://doi.org/10.21508/1027-4065-2022-67-6-68-74
Abstract
The purpose of the study was to evaluate the course and outcome in chronic kidney disease of congenital anomalies of the kidneys and urinary tract (CAKUT) associated with rare hereditary syndromes in children and adolescents, and to compare the results with literature data. The results of a follow-up study of the course and outcome in chronic kidney disease with syndromal congenital anomalies of the kidneys and urinary tract in rare hereditary syndromes (Pierson, Fraser 1 type, Renal hypodysplasia/ aplasia 3 type, Schuurs– Hoeómakers, CHARGE, Lowe, Renal-Coloboma, VACTERL association) and chromosomal abnormalities (Shereshevsky—Terner monosomia 45) are presented. In 4 out of 9 children and adolescents with congenital anomalies of the kidneys and urinary tract with rare hereditary syndromes, the formation of chronic kidney disease was established.
About the Authors
I. E. Kutyrlo
Saint Petersburg State Pediatric Medical University; City Polyclinic No. 114; Children’s Polyclinic Department No. 70
Russian Federation
Russian Federation
Saint Petersburg
Zh. G. Leviashvili
Saint Petersburg State Pediatric Medical University
Russian Federation
Russian Federation
Saint Petersburg
D. D. Batrakov
Saint Petersburg State Pediatric Medical University
Russian Federation
Russian Federation
Saint Petersburg
N. D. Savenkova
Saint Petersburg State Pediatric Medical University
Russian Federation
Russian Federation
Saint Petersburg
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Review
For citations:
Kutyrlo I.E., Leviashvili Zh.G., Batrakov D.D., Savenkova N.D. Follow-up of children and adolescents with congenital anomalies of the kidneys and urinary tract, associated with rare hereditary syndromes. Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics). 2022;67(6):68-74. (In Russ.) https://doi.org/10.21508/1027-4065-2022-67-6-68-74
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