Literature DB >> 24057736

A rare association of diphallus, colonic duplications, ileal atresia, and an anorectal malformation.

S P Sharma1, A N Gangopadhyay, D K Gupta, S Chooramani Gopal, R N Dash, C K Sinha.   

Abstract

Diphallus is a rare congenital anomaly that is often associated with various other anomalies of the midline structures of the posterior portion of the body. We report a unique case of a 1-day-old male with complete diphallus, incomplete bilateral tubular duplications of the colon, ileal atresia, and an anorectal malformation.

Entities:  

Year:  2013        PMID: 24057736     DOI: 10.1007/BF00497833

Source DB:  PubMed          Journal:  Pediatr Surg Int        ISSN: 0179-0358            Impact factor:   1.827


  4 in total

1.  Value of sonography in true complete diphallia.

Authors:  L Marti-Bonmati; F Menor; J Gomez; H Cortina; F Garcia Ibarra
Journal:  J Urol       Date:  1989-08       Impact factor: 7.450

2.  Embryologic considerations of diphallus and associated anomalies.

Authors:  J G Hollowell; R Witherington; A J Ballagas; J N Burt
Journal:  J Urol       Date:  1977-06       Impact factor: 7.450

3.  Diphallia: report of a case.

Authors:  A A Aleem
Journal:  J Urol       Date:  1972-08       Impact factor: 7.450

4.  Complete duplication of the bladder, urethra and external genitalia in a neonate--a case report.

Authors:  R Kapoor; M M Saha
Journal:  J Urol       Date:  1987-06       Impact factor: 7.450

  4 in total
  1 in total

Review 1.  Diphallia: literature review and proposed surgical classification system.

Authors:  Dylan John Kendrick; Roy Mark Kimble
Journal:  ANZ J Surg       Date:  2022-06-09       Impact factor: 2.025

  1 in total

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