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International Journal of Medical Paediatrics and Oncology
Year : 2017, Volume : 3, Issue : 3
First page : ( 136) Last page : ( 136)
Print ISSN : 0000-000X. Online ISSN : 2455-6793.
Article DOI : 10.18231/2455-6793.2017.0030

Complete Diphallia with no other associated congenital anomaly

Sharma Nandini1,*, Gupta Sonal1, Goyal Mohit1, Sattavan Sunita1

1Resident, Dept. of Pediatrics, MG Medical College & Hospital, Jaipur, Rajasthan

*Corresponding Author: Email: drnandinisharma09@gmail.com

Online published on 23 February, 2018.

Abstract

We report a case of Diphallus in a term-appropriate for gestational age, male child weighing 3.1 kg with abnormal genitalia i.e. double penises one below the other with normal scrotum and normal sized testis. No other congenital anomaly was apparent. USG revealed single urinary bladder and normal intra abdominal organs. Baby was voiding through the bottom penis. MCU revealed a single urinary bladder with duplication of the urethra with a blind end in the orthotopic penis. There was no evidence of VUR. Surgical treatment was offered. However, unfortunately the patient was lost on follow up.

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