Congenital hydronephrosis refers to the swelling (dilation) of the kidney’s drainage system due to urine buildup. It is often discovered during routine prenatal ultrasounds and varies from mild to severe depending on the cause and extent of obstruction or urine backflow.
Types of Congenital Hydronephrosis
1. Physiologic (Transient) Hydronephrosis
Temporary and often resolves spontaneously without treatment.
2. Obstructive Hydronephrosis
Caused by physical blockage, such as:
Ureteropelvic junction (UPJ) obstruction
Ureterovesical junction (UVJ) obstruction
Posterior urethral valve (PUV)
3. Reflux-related Hydronephrosis
Due to vesicoureteral reflux (VUR), where urine flows backward from the bladder to the kidney.
Symptoms of Congenital Hydronephrosis
Many infants are asymptomatic and diagnosed via imaging.
What Causes Congenital Hydronephrosis?
- Developmental abnormalities in the urinary tract during fetal growth
- Obstructive lesions (e.g., UPJ obstruction, PUV)
- Genetic predisposition or family history of urinary tract malformations
- Male gender (higher incidence)
Prevention of Congenital Hydronephrosis
Although the condition itself cannot be prevented, early detection through routine prenatal ultrasound enables close monitoring and timely management, reducing the risk of kidney damage.