Results 81 to 90 of about 1,398,641 (158)

Doença do nó sinusal em paciente jovem com síndrome de Mayer-Rokitansky-Küster-Hauser [PDF]

, 2017
Relato do caso de uma paciente de 39 anos de idade com síndrome de Mayer-Rokitansky-Küster-Hauser, apresentando doença do nó sinusal e necessidade de implante de marcapasso bicameral.
Marcel Pereira Moussa, Cristiano de Oliveira Dietrich, André Soares Maria, Luciana Vidal Armaganijan   +3 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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Leiomioma uterino en paciente con síndrome de Mayer-Rokitansky-Küster-Hauser: reporte de caso Uterine leiomyoma in a patient suffering from Mayer-Rokitansky-Küster-Hauser syndrome: A case report

Revista Colombiana de Obstetricia y Ginecología, 2010
Objetivo: el síndrome de Mayer-Rokitansky-Küster-Hauser (MRKH) es una malformación congénita del útero y la parte superior de la vagina en las mujeres que muestran características sexuales secundarias normales y cariotipo 46 XX.
Mario Arturo González-Mariño, Mario Pérez-Solano   +1 more
doaj  

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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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

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
doaj  

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 (MRKH) syndrome. Diagnostic and therapeutic approach of a rare disease

, 2019
Introduccion: El síndrome de Mayer-Rokitansky-Küster-Hauser se caracteriza por la agenesia de vagina y útero en una mujer con desarrollo normal de caracteres sexuales y amenorrea primaria.
Martín, Silvia, Noguero, Rosario, Muñoz, María del Mar   +2 more
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Mayer-Rokitansky-Küster-Hauser syndrome type II: a case report and literature review [PDF]

Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is a genetic disease consisting of absent uterus and upper part of vagina, and is seen in women with a normal karyotype (46, XX). It is one of the rare diseases where the estimated prevalence is 1:5000. Most
Baishya, Kakoli, Baishya, Nirupam K., Pathak, Jyotishmita   +2 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