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

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 vagina...

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Detalles Bibliográficos
Autores principales: Belkhode, Vikram Murlidhar, Nimonkar, Sharayu Vinod
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8309006/
https://www.ncbi.nlm.nih.gov/pubmed/34367422
http://dx.doi.org/10.11604/pamj.2021.38.343.28837
Descripción
Sumario: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.

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