Congenital aphallia is a rare anomaly with little supporting literature and controversial
management. The aim of this review is to assess the most recent literature with a focus on …

Background Aphallia is a rare congenital anomaly often associated with other urogenital
anomalies. The management of aphallia cases for both the immediate and long-term …

Introduction Aphallia is exceedingly rare (1/30 million births). Previous reports have
provided limited detail on associated urinary tract findings. Objective We reviewed urinary …

Background: Aphallia or penile agenesis is a rare malformation accompanying with no
phallus. This anomaly is extremely rare with abnormality of urogenital system and …

Aphallia or penile agenesis is very rare congenital anomaly of unknown cause occurring 1
in 30 million live births. Very little has been written in literature about aphallia. There is …

Aphallia or penile agenesis is a rare case of the genitourinary system which has an
association with upper urinary tract disorder. Failure of fetal genital tubercle formation in the …

Aphallia or penile agenesis is a rare congenital malformation with an estimated incidence
rate of 1 in 10 to 30 million births. More than half of aphallia cases have associated …

BACKGROUND: Congenital aphalia is an extremely rare, urogenital malformation of the
external genitalia characterized by congenitally absent penis in a karotypically XY child. It …

Congenital penile agenesis is a rare condition with an incidence of 1 in 30 million, while
other congenital malformations of the cavernous bodies are much less common. In a few …

Aphallia, or agenesis of the penis, is a very rare congenital anomaly, with an estimated
incidence of one in every 10-30 million births. More than half of aphallia cases have …