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.
Highlights
Кистозные дисплазии представляют гетерогенную группу заболеваний, на долю которых в структуре врожденных аномалий почек приходится 12–15%, а в структуре причин хронической почечной недостаточности у детей – 8–10%
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
Summary
Кистозные дисплазии представляют гетерогенную группу заболеваний, на долю которых в структуре врожденных аномалий почек приходится 12–15%, а в структуре причин хронической почечной недостаточности у детей – 8–10%. Autosomal Recessive Polycystic Kidney Disease in the Structure of Cystic Dysplasia in Children For citation: 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. Аутосомно-рецессивный поликистоз почек в структуре кистозных дисплазий у детей
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