Results 61 to 70 of about 262,079 (155)

Detection of de novo genetic variants in Mayer–Rokitansky–Küster–Hauser syndrome by whole genome sequencing

European Journal of Obstetrics & Gynecology and Reproductive Biology: X, 2019
Objective: The aim of this study was to use whole genome sequencing (WGS) help detect de novo mutations or pathogenic genes of Mayer-Rokitansky-Küster-Hauser syndrome type 1(MRKH syndrome type 1). Study design: This was a case-parent trios study.
Hong-xin Pan, Guang-nan Luo, Sheng-qing Wan, Cheng-lu Qin, Jie Tang, Meng Zhang, Min Du, Ke-ke Xu, Jin-qiu Shi   +8 more
doaj   +1 more source

Prolapse and sexual function 8 years after neovagina according to Shears: a study of 43 cases with Mayer-von Rokitansky-Küster-Hauser syndrome [PDF]

, 2013
To investigate sexual and anatomical outcome after Shears neovagina in patients with Mayer-von Rokitansky-Kuster-Hauser syndrome (MRKH)
Im Obersteg, Jeannine, Kuhn, Annette, Neukomm, Corinne, Dreher, Ekkehard F, Mueller, Michael D   +4 more
core   +2 more sources

How do women with Rokitansky syndrome and healthcare professionals reflect on the provision of uterine transplantation? Insights from an interview study in France, Norway, and Sweden

Acta Obstetricia et Gynecologica Scandinavica
Introduction Uterine transplantation is currently intended for women with absolute uterine infertility. Since proof of the concept in 2014, many countries have started research programs and clinical activities.
Isis Carton, Ludivine Dion, Vincent Lavoué, Bjorn Morten Hofmann   +3 more
doaj   +1 more source

Syndrome de Mayer-Rokitansky-Küster-Hauser

PAMJ Clinical Medicine, 2019
Le syndrome de Mayer-Rokitansky-Küster-Hauser est une malformation rare de la filière génitale chez la femme qui se définit par l’agénésie de l’utérus et du vagin mais avec des ovaires normaux.
Hassan Doulhousne, Zakaria Toufga, Abdelilah Mouhsine, Mehdi Atmane   +3 more
doaj   +1 more source

Toward Next‐Generation Teratology: Understanding Developmental Vulnerability Through Evolutionary and Comparative Genomics

Congenital Anomalies, Volume 66, Issue 1, January/February 2026.
ABSTRACT Teratology, the study of congenital anomalies, has developed from a descriptive discipline into a mechanistic science focused on the proximate causes of developmental defects, meaning how such anomalies arise during development. However, a comprehensive understanding requires not only this mechanistic insight but also an evolutionary ...
Tetsuo Kon
wiley   +1 more source

Síndrome de Mayer-Rokitansky-Küster-Hauser o agenesia de útero y vagina en una paciente joven [PDF]

, 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 ...
Orozco Hechavarría, Nélida, Baralt Ross, Juana Himilce, Prades Hung, Eliecer   +2 more
core   +1 more source

Leiomioma uterino en paciente con síndrome de Mayer-Rokitansky-Küster-Hauser: reporte de caso

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   +3 more sources

Vaginoplasty with Amnion Graft: Management of Mayer-Rokitansky-Kuster-Hauser Syndrome

Journal of Nepal Health Research Council
Mayer-Rokitansky-Kuster-Hauser syndrome also known as mullerian agenesis is a rare congenital condition in which there is absence of uterus along with upper vagina.
Srijana Bhandari, Ganesh Dangal, Aruna Karki, Hema Pradhan, Ranjana Shrestha, Kabin Bhattachan, Kenusha Devi Tiwari, Sonu Bharati, Sunita Maharjan   +8 more
doaj   +1 more source

Descripción de técnica simplificada de neovagina. Reporte de 4 casos. Cali (Colombia)

Revista Colombiana de Obstetricia y Ginecología, 2010
Introducción: la agenesia de vagina representa una malformación infrecuente cuyas principales causas son el síndrome de Rokitansky-Mayer-Kuster-Hauser y la insensibilidad a los andrógenos o síndrome de feminización testicular.
Gustavo Gómez-Tabares, Albaro José Nieto-Calvache   +1 more
doaj   +1 more source

Malformations in a cohort of 284 women with Mayer-Rokitansky-Küster-Hauser syndrome (MRKH) [PDF]

, 2012
Background The aim of this retrospective study was to describe the spectrum of genital and associated malformations in women with Mayer-Rokitansky-Küster-Hauser syndrome using evaluated diagnostic procedures and the Vagina Cervix Uterus Adnex ...
Strick, Reiner, Rall, Katharina, Schulze, Christine, Schulze Christine, Johannes Lermann, Matthias W Beckmann, Reiner Strick, Dittrich, Ralf, Strissel, Pamela, Rall Katharina, Oppelt Patricia G, Oppelt, Patricia G., Beckmann, Matthias W., Dittrich Ralf, Sara Brucker, Strick Reiner, Rettig Ingo, Beckmann Matthias W, Andreas Mueller, Lermann, Johannes, Katharina Rall, Patricia G Oppelt, Ralf Dittrich, Renner, Stefan P., Brucker, Sara, Ingo Rettig, Rettig, Ingo, Mueller, Andreas, Brucker Sara, Mueller Andreas, Pamela Strissel, Lermann Johannes, Stefan P Renner, Christine Schulze, Strissel Pamela, Renner Stefan P   +35 more
core   +1 more source