Congenital Anomalies of the Urinary Tract
Also known as: congenital anomalies of the kidney and urinary tract, CAKUT, congenital genitourinary anomalies, bladder anomalies, congenital urogenital malformations
What are congenital anomalies of the urinary tract?
Congenital anomalies of the urogenital tract, are a broad group of common, mild to life-threatening malformations (approx. 30% of all prenatally diagnosed malformations) of the kidney/ureters/bladder/urethra/penis/testis/and female genitalia (one or more parts) present at birth that occur during fetal development of the urinary/genital system.
They are often accompanied by other birth defects outside the kidney's/collecting system (ureters/bladder/urethra). Several are part of a “syndrome” (a collection of signs and symptoms that usually are found together); some are not (“non-syndromic”).
In young children CAKUT are a leading cause of kidney failure and renal transplantation.
What causes congenital anomalies of the urinary tract?
Causes vary; some appear to be genetic (inherited), in others environment may play a role.
What are the signs/symptoms of congenital anomalies of the urinary tract?
Symptoms of congenital anomalies of the urinary/genital tract vary widely depending on what part of the urinary/genital system is affected and whether other body systems are involved.
What are congenital anomalies of the urinary tract care options?
While some congenital anomalies of the urinary/genital tract do not cause any symptoms, and require no treatment, others depending on a variety of factors may require extensive medical and surgical interventions.
Reviewed by: Jack Wolfsdorf, MD, FAAP
This page was last updated on: May 01, 2020 04:37 PM
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