https://www.selleckchem.com/products/ikk-16.html
Aphallia is an extremely rare congenital malformation of unknown cause, with few reports in the literature. It is usually associated with other urogenital and gastrointestinal anomalies and is believed to be a result of either the absence of a genital tubercle or chromosome polymorphism. Herein, we describe an extremely rare case of congenital aphallia with congenital urethrorectal fistula and describe our treatment for this patient. An 8-year-old boy was brought to our hospital by his parents because of congenital absence of the penis.
Like
Comment
Share
