Congenital Cystic Renal Dysplasia

By the term “congenital cystic renal dysplasia” congenital malformations including. metanephrischer malformations or congenital obstructive uropathies summarized.

(See also Overview of cystic Nierenerkrankheiten.)

By the term “congenital cystic renal dysplasia” congenital malformations including. metanephrischer malformations or congenital obstructive uropathies summarized. (See also Overview of cystic Nierenerkrankheiten.) A congenital renal cystic dysplasia affects one or both kidneys. A renal cystic dysplasia, an isolated congenital anomaly or part of a malformation syndrome (i.e. h in conjunction with other clinical features -see Table:.. Main groups of cystic nephropathies). Among the related urological abnormalities Ureterabgangs can – and Uretermündungsstenose, neurogenic bladder, Ureterocele, posterior urethral valves and prune belly syndrome (characterized by muscular abdominal wall defect, Harntraktfehlbildung [e.g., dilated ureters, advanced bladder and urethra.] And bilateral cryptorchidism ). Symptoms and complaints vary depending on how much kidney function tissue is obtained, and whether the events on one or both sides. To a certain extent to renal failure or kidney failure can develop. In general, congenital cystic renal dysplasia is detected by ultrasound prenatally or during early childhood. Because of the difficulty of assessing the remaining functioning renal parenchyma, the prognosis is difficult to predict. Treatment consists of surgical correction of accompanying urogenital anomalies and when a renal or even kidney failure has arisen in renal replacement therapy.

Health Life Media Team

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