Affiliation:
1. Pediatric B Department–Mother-Child Pole, Mohammed VI University Hospital, Marrakesh, Morocco
Abstract
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 anomalies including caudal axis, cardiovascular, genitourinary, and gastrointestinal anomalies. The penile agenesis associated with adrenal insufficiency has never been reported in an infant. We report a rare case of a newborn that was diagnosed as a case of aphallia with vesicorectal fistula and vesicoureteral reflux, complicated by adrenal insufficiency with salt-wasting crisis.
Reference6 articles.
1. A rare case of aphallia with right kidney hypoplasia and left kidney dysplasia;S. Aslanabadi;Archives of Iranian Medicine,2015
2. Agenesis of penis
3. A case report of aphallia with urorectal septum malformation sequence in a newborn: a very rarely seen condition
4. Aphallia: a very rare congenital anomaly, with associated genitourinary and ano-rectal malformation;M. U. Nisar;Journal of Ayub Medical College Abbottabad,2018
5. Congenital absence of the penis (aphallia)
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