Penile agenesis or aphallia is a rare congenital anomaly occurring with a frequency of 1:10 -1:30 million newborns. Fewer than 100 cases have been reported worldwide. Associated urogenital malformations and the presence of oligohydramnios with pulmonary hypoplasia determine the infant's viability. Extra-urogenital anomalies have been described in the cardiovascular, gastro-intestinal and muscul...

introduction: aphallia is a very rare urogenital anomaly with incidence rate of 1 in 30,000,000. it usually coexists with other anomalies such as cardiovascular anomalies which are incompatible with normal life, and therefore infants are delivered stillbirth or live for a very short period of time. methods: we present an 18 months old boy with aphallia associated with congenital urethrorectal f...

background: aphallia or penile agenesis is a rare malformation accompanying with no phallus. this anomaly is extremely rare with abnormality of urogenital system and psychological consequences. its outbreak is estimated 1 out of 10-30 million births.case: reviewing 3 cases of male external genitalia agenesis, which associated with multiple anomalies of musculoskeletal, cardiovascular and genito...

During the most recent years, a variety of new techniques of penile reconstruction have been described in the literature. This paper focuses on the most recent advances in male genital reconstruction after trauma, excision of benign and malignant disease, in gender reassignment surgery and aphallia with emphasis on surgical technique, cosmetic and functional outcome.

Abstract Background Aphallia is a rarest of rare congenital anomaly the incidence being 1 in 10 to 30 million live births. Seen at birth, it leaves parents and family disturbed. Immediate counselling though done; may take time for come decision. Case presentation A newborn was brought genital examination since penis not present scrotum with testes were normal, aphallia suspected. At month after...