• Up to 4 types have been described: Type 1 (the most common): two mucosal folds at the level of the verumontanum with a ventral central slit-like orifice Type 3: this has a pin-point, eccentric orifice which results in forward ballooning of the valve, giving a ‘wind in the sail’ appearance on an oblique MCUG projection there is a high association with renal dysplasia and minimal upper tract dilatation • Recto-urethral fistula: this rare abnormality is usually associated with an imperforate anus air within the bladder confirms the diagnosis • Urethral duplication: there is usually complete duplication with one of the urethras ending as a hypospadias • Hypospadias: absence of the ventral aspect of the distal urethra • Epispadias: absence of the dorsal aspect of the distal urethra
Urethra
URETHRA: BENIGN DISORDERS
CONGENITAL ANOMALIES
Clinical presentation
Other urethral anomalies