Abstract

Among the anomalies in the development of all organs and systems, congenital malformations of the kidneys and upper urinary tract occupy the first place, accounting for 12.9–40% of all congenital malformations and 3–5.5% of the total number of urological cases. The combination of two or more anomalies of the genitourinary system is extremely rare. The article presents a description of the clinical observation and the choice of surgical treatment for three anomalies in the development of the urinary system, for a long time unrecognized in a 19-year-old patient — pelvic dystopia of the left hypoplastic kidney with vaginal ectopia of the ureter.

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