Results 91 to 100 of about 1,398,641 (158)

Mayer-Rokitansky-Küster-Hauser Syndrome or uterus and vagina agenesis in a young patient

open access: yesMedisan, 2018
The case report of a patient with syndrome of Mayer-Rokitansky-Küster-Hauser or uterus and vagina agenesis, but with functioning ovaries, assisted by a multidisciplinary team in "Tamara Bunke Bider" Northern Maternal Hospital in Santiago de Cuba, whose ...
Juana Himilce Baralt Ross   +2 more
doaj  

Síndrome de Mayer-von Rokitansky-Küster-Hauser

open access: yes, 2018
Introduction: The Mayer-von Rokitansky-Küster-Hauser (MRKH) syndrome happens in approximately one of 5000 women born alive and is the commonest cause of congenital absence of the vagina.Method:We present two cases handled surgically by means of abdomino ...
Lombana, Luis Jorge; Pontificia Universidad Javeriana   +2 more
core  

Vaginoplastia Sigmoide Mini-Laparoscópica na Síndrome de Mayer-Rokitansky [PDF]

open access: yes, 2017
Mayer-Rokitansky-Küster-Hauser syndrome describes a vaginal and uterine agenesis, secondary to agenesis or hypoplasia of the Müllerian duct system.
Bailez, Marcela   +4 more
core  

Adolescente con síndrome de Mayer-von Rokitansky-Küster-Hauser: la importancia de un manejo integral multidisciplinario An adolescent suffering from Mayer-von Rokitansky-Küster-Hauser syndrome: the importance of an integral multidisciplinary approach

open access: yesRevista Colombiana de Obstetricia y Ginecología, 2006
Se presenta el caso clásico de una adolescente con diagnóstico incidental y tardío de síndrome de Mayer-von Rokitansky-Küster-Hauser y lo que consideramos aspectos fundamentales a tener en cuenta para favorecer el diagnóstico precoz y manejo de estas ...
Gabriel Barbosa, Mario Varela-Guzmán
doaj  

Inguinal Ovarian Herniation Revealing Mayer-Rokitansky-Küster-Hauser Syndrome Type B- A Case Report

open access: yes
Inguinal ovarian herniation is an uncommon finding in adult women and may be associated with congenital Müllerian anomalies such as Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome.
Mehdi Salmane   +5 more
core   +1 more source

Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome - a review

open access: yesIndian Journal of Urology, 2002
Purpose: Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is a congenital malformation characterized by an absence of the vagina associated with a variable abnormality of the uterus and the urinary tract butfunc-tional ovaries. We review the embryological,
N P Gupta, M S Ansari
doaj  

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