Hostname: page-component-68c7f8b79f-p5c6v Total loading time: 0 Render date: 2025-12-20T11:04:03.771Z Has data issue: false hasContentIssue false
  • English
  • Français

Correspondence: Case report: congenitalurethrocutaneous fistula

Published online by Cambridge University Press:  01 January 1997

J. BARWELL  and
D. HARRIS
J. BARWELL
Affiliation:
Department of Plastic Surgery, Derriford Hospital, Plymouth PL6 8DH, UK
D. HARRIS
Affiliation:
Department of Plastic Surgery, Derriford Hospital, Plymouth PL6 8DH, UK

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

A 2-year-old boy presented with a suspected urethrocutaneous fistula. He had been born at 26 wk gestation and spent 14 wk in the special care baby unit with severe respiratory problems and an episode of meningitis. He had not had a urinary catheter in situ or urinary tract infections. Bilateral inguinal hernias had been repaired. At presentation he was below the 3rd centile for height and weight but had reached all other developmental milestones.

Information

Type
Letter
Information
The Journal of Anatomy , Volume 190 , Issue 1 , January 1997 , pp. 155 - 156
Copyright
© Anatomical Society of Great Britain and Ireland 1997