[Mayer-Rokitansky-Küster-Hauser syndrome. A case report and a review of the medical literature on its treatment]. / Sindrome de Mayer-Rokitansky-Küster-Hauser. Reporte de un caso y revisión de la bibliografía relacionada con su tratamiento.
Ginecol Obstet Mex
; 80(7): 473-9, 2012 Jul.
Article
em Es
| MEDLINE
| ID: mdl-22916641
The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome affects 1 out of 4500 women. It is characterized by the congenital absence of the upper third of the vagina, uterus and tubes; it is usually associated to renal malformations, and patients show normal phenotype and genotype. Age at diagnosis is between 15 and 18. A case is reported and a critical review of the information about the management alternatives of patients with MRKH syndrome available in medical literature is made. The paper is intended to help establish the best criteria and treatment options for a comprehensive therapeutic approach to MRKH patients.
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Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Anormalidades Múltiplas
/
Transtornos 46, XX do Desenvolvimento Sexual
Tipo de estudo:
Diagnostic_studies
Limite:
Adolescent
/
Female
/
Humans
Idioma:
Es
Revista:
Ginecol Obstet Mex
Ano de publicação:
2012
Tipo de documento:
Article
País de publicação:
México