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Hollow vaginal stent for a case of Mayer-Rokitansky-Kuster-Hauser syndrome: a case report.

Abstract
Congenital vaginal agenesis is a common condition with an instance of 1 in 5000 females. It is usually associated with Mayer-Rokitansky-Kuster Hauser syndrome. Such anomalies have a high impact on the physiology and psychology of patients. A simple approach for the hollowing of the customized vaginal stent prosthesis has been described for the case of Mayer-Rokitansky-Kuster-Hauser syndrome.
AuthorsVikram Murlidhar Belkhode, Sharayu Vinod Nimonkar
JournalThe Pan African medical journal (Pan Afr Med J) Vol. 38 Pg. 343 ( 2021) ISSN: 1937-8688 [Electronic] Uganda
PMID34367422 (Publication Type: Case Reports)
CopyrightCopyright: Vikram Murlidhar Belkhode et al.
Topics
  • 46, XX Disorders of Sex Development (surgery)
  • Adolescent
  • Congenital Abnormalities (surgery)
  • Female
  • Humans
  • Mullerian Ducts (abnormalities, surgery)
  • Prosthesis Design
  • Prosthesis Implantation (methods)
  • Stents

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