Journal of the Pakistan Medical Association (Feb 2024)

Caudal duplication syndrome: a rare entity

  • Saadia Kanwal,
  • Shazia Batool,
  • Shamoona Naqvi,
  • Naila Israr,
  • Samina Akhtar,
  • Saadia Zia

DOI
https://doi.org/10.47391/JPMA.8664
Journal volume & issue
Vol. 74, no. 4

Abstract

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The rare caudal duplication syndrome is a spectrum of anomalies primarily involving partial or complete duplication of organs comprising the gastrointestinal, genitourinary and distal neural tube systems. These findings are considered to be a result of aberrant embryogenesis. We hereby report a case of an adult female with complete duplication of the genital and urinary systems (urethra and bladder), hindgut and lower end of vertebral column with no functional impairment. She presented in her first pregnancy at 36 weeks gestation, in labour. To the author's knowledge this is the first case of caudal duplication syndrome with pregnancy from Pakistan. Key Words: Caudal duplication, Genitourinary, Gestation, Hindgut.

Keywords