Clinical case of urethral doubling with preservation of function and single bladder

Urethral doubling is a rare congenital anomaly of the urinary system that more common in boys. Less than 500 clinical cases this disease have been described literature, which may signal lack awareness among physicians. Although there are many considerations regarding embryology anomaly, etiopathogenesis its various forms remains unclear. Sometimes urethra combined with other malformations, such as epispadias, hypospadias, exstrophy bladder, anorectal malformation, bladder and others. In article, we present case 9-year-old boy urethral duplication additional epispadias. We found main urethra, goes on dorsal side penis led to curvature incontinence. During operation, urethrocystoscopy was performed before stage, complete type 2-A established according Effman classification, after excised far pubic bones. several presentation, often accompanied by anomalies, sometimes difficult diagnosis. The treatment should be individualized, type. find IIa, has treated classic Therefore, child malformation need perform obsrvetion like urethrography, cystoscopy. research carried out accordance principles Helsinki Declaration. informed consent patient obtained for conducting studies. No conflict interests declared authors. Key words: substitution,