AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY DISEASE IN THE STRUCTURE OF CYSTIC DYSPLASIA IN CHILDREN
https://doi.org/10.21508/1027-4065-2018-63-5-172-176
Abstract
Cystic dysplasia is a heterogeneous group of diseases, with 12–15% share in the structure of congenital kidney anomalies and 8–10% share in the structure of the causes of chronic renal failure in children. The article presents the results of observation of patients with polycystic kidney disease. To study the clinical features of the course of various forms of cystic dysplasia in children we analyzed the histories of children with autosomal recessive and autosomal dominant polycystic kidney disease. We revealed clinical, laboratory and instrumental features of the course of various types of cystic renal dysplasia.
About the Authors
T. P. MakarovaRussian Federation
V. P. Bulatov
Russian Federation
N. V. Samoylova
Russian Federation
G. M. Samoylova
Russian Federation
L. V. Poladova
Russian Federation
I. N. Cherezova
Russian Federation
Yu. S. Melnikova
Russian Federation
References
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Review
For citations:
Makarova T.P., Bulatov V.P., Samoylova N.V., Samoylova G.M., Poladova L.V., Cherezova I.N., Melnikova Yu.S. AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY DISEASE IN THE STRUCTURE OF CYSTIC DYSPLASIA IN CHILDREN. Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics). 2018;63(5):172-176. (In Russ.) https://doi.org/10.21508/1027-4065-2018-63-5-172-176