IMR Press / CEOG / Volume 26 / Issue 3-4 / pii/1999052

Clinical and Experimental Obstetrics & Gynecology (CEOG) is published by IMR Press from Volume 47 Issue 1 (2020). Previous articles were published by another publisher on a subscription basis, and they are hosted by IMR Press on imrpress.com as a courtesy and upon agreement with S.O.G.

Case Report

Penis, bladder and uretral agenesis associated with anorectal malformation in a living male neonate

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1 Department of Pediatric Surgery Catania University, Italy
2 Department of Obstetrics, Casa di Cura Villa Aurora, Reggio Calabria, Italy
3 Hematologic and Genetic Laboratory, Reggio Calabria, Italy
Clin. Exp. Obstet. Gynecol. 1999, 26(3-4), 225–226;
Published: 10 September 1999
Abstract

Aphallia is a very rare congenital malformation, with an occurrence of 1 in every 30 million births. In the international literature about 75 cases have been indicated as of today. The authors report and discuss the case of one neonate, born from a monoamniotic twin delivery, suffering from agenesis of the penis, anorectal malformation with a fully formed scrotum with 2 normal gonads and absence of bladder and urethra and both kidneys.

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