Results 81 to 90 of about 262,079 (155)

Síndrome de Mayer-Rokitansky-Küster-Hauser (MRKH). Enfoque diagnóstico y terapéutico de un cuadro poco frecuente. [PDF]

, 2011
Introduction: The Mayer-Rokitansky-Küster-Hauser syndrome is characterized by the absence of the vagina and uterus and primary amenorrhea. Objective: The diagnostic evaluation and the therapeutic possibilities of a rare syndrome. Materials and methods:
Martín, Silvia, Noguero, Rosario, Muñoz, María del Mar   +2 more
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Síndrome de Mayer-von Rokitansky-Küster-Hauser

, 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, Quintero, Leila; Pontificia Universidad Javeriana, Barbosa Ramírez, Gabriel Andrés; Pontificia Universidad Javeriana   +2 more
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Specific problems of nursing patients suffering from Mayer-Rokitansky-Küster-Hauser syndrome [PDF]

, 2012
W pracy przedstawiono opis przypadku chorej z zespołem Mayera-Rokitansky'ego-Küstera-Hausera. Scharakteryzowano czynniki etiologiczne, obraz kliniczny, diagnostykę i metody leczenia.
Kopański, Zbigniew, Gontarczyk, K., Kozłowska, D.   +2 more
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Supplementary Material for: Identification of Candidate Genes for Mayer-Rokitansky-Küster-Hauser Syndrome Using Genomic Approaches

, 2018
Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is a disorder of sex development which affects 1 in 4,500 females and is characterized by agenesis of müllerian structures, including the uterus, cervix, and upper vagina.
Simons C. (6036696), Backhouse B. (6036687), Grover S. (4126339), Ayers K. (6036703), Pelosi E. (6036695), Koopman P. (4127185), Juniarto A.Z. (6036698), van den Bergen J. (6036693), Robevska G. (6036692), Faradz S. (6036699), Tan T.Y. (3116835), Hanna C. (6036690), Sinclair A. (6036701)   +12 more
core   +1 more source

Síndrome de Mayer-Rokitansky-Küster-Hauser (MRKH). Enfoque diagnóstico y terapéutico de un cuadro poco frecuente

, 2012
Introduction: The Mayer-Rokitansky-Küster-Hauser syndrome is characterized by the absence of the vagina and uterus and primary amenorrhea. Objective: The diagnostic evaluation and the therapeutic possibilities of a rare syndrome. Materials and methods:
DEL MAR MUÑOZ, MARÍA, MARTÍN, SILVIA, NOGUERO, ROSARIO   +2 more
core   +1 more source

Bilateral indirect ovarian inguinal hernia in a young female with type 1 Mayer–Rokitansky–Küster–Hauser syndrome: An extremely rare clinical context

Clinical Case Reports
Key Clinical Message Incidence of bilateral inguinal hernia encompassing bilateral ovaries in adult female is very thin and concomitant association with Mayer–Rokitansky–Küster–Hauser syndrome is out of ordinary. Along with surgical management of hernia,
Sunil Bhatta, Hemant Ojha, Meraj Alam Ansari, Anuj Shrestha   +3 more
doaj   +1 more source

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

Medisan, 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, Nélida Orozco Hechavarría, Eliecer Prades Hung   +2 more
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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

Revista 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
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Exploring the psychological impact of Mayer-Rokitansky-Kuster-Hauser syndrome on young women: an interpretative phenomenological analysis

, 2016
This study explored five young women’s experiences of living with Mayer–Rokitansky–Küster–Hauser to offer a unique insight into the social challenges of Mayer–Rokitansky–Küster–Hauser in the transition to adulthood.
Patterson, Carolyn J., Jahoda, Andrew, Carolyn J Patterson, Rebecca Crawford, Crawford, Rebecca, Andrew Jahoda   +5 more
core   +1 more source

Mayer-Rokitansky-Kuster-Hauser syndrome: a review

International Journal of Women's Health, 2015
Laura Londra, Farah S Chuong, Lisa KolpDivision of Reproductive Endocrinology and Infertility, Department of Gynecology and Obstetrics, Johns Hopkins University, Baltimore, MD, USAAbstract: The congenital aplasia or severe hypoplasia of mullerian ...
Londra L, Chuong FS, Kolp L
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