Fetal hydronephrosis as one of the most common abnormalities that has occurred in fetals, affecting 0.17 to 2.3% of pregnancies, is found in the prenatal ultrasound examination (
1,
2). It occurs as kidney swelling due to failure of normal drainage of the urine from the kidney to the bladder (
3,
4). This condition commonly affects only 1 kidney, however, it may involve both kidneys (
5,
6). Hydronephrosis is not a primary condition and results from other underlying diseases that result from a blockage or obstruction in the urinary tract (
7-
9). Acute unilateral obstructive uropathy is one of the most common causes of hydronephrosis, other causes include a torsion of ureteropelvic junction, tumors in or near the ureter, and narrowing of the ureter from congenital defect or injury (
2,
10,
11). Clinical manifestations are based on the duration of obstruction; mild symptoms include frequently urinating and increase in urge to urinate (
12-
14). Other potential symptoms include abdominal or flank sharp pain, nausea, vomiting, incomplete voiding, urinating, pain, and fever (
15,
16). This has been diagnosed by an ultrasonography, and since treatment focuses on getting rid of blocking flow of urine based on the obstruction reasons, it represents a transient condition that resolves maturation of tubular function, increasing ability of reabsorption, and maturation of ureteropelvic junction in the kidney (
3,
17,
18). Based on this content, hydronephrosis has a high prevalence in children and its etiology varies in different studies. Therefore, the aim of this was an etiology evaluation in neonates with hydronephrosis.