Results 71 to 80 of about 262,079 (155)

Mayer-Rokitansky-Kuster-Hauser Syndrome Associated with Severe Inferior Vena Cava Stenosis

Case Reports in Obstetrics and Gynecology, 2014
Precis. The postoperative course of a neovagina creation procedure in a young woman with Meyer-Rokitansky-Kuster-Hauser syndrome was complicated, despite prophylaxis, by extensive pelvic deep venous thrombosis secondary to unsuspected severe inferior ...
Laura Londra, Kyle Tobler, John Wu, Lisa Kolp   +3 more
doaj   +1 more source

Primary Amenorrhea With Bilateral Endometriomas in a Teenager Girl With Cervical Hypoplasia and Vaginal Agenesis

Clinical Case Reports, Volume 14, Issue 2, February 2026.
Shahzeen Irshad, Maryam Irshad, Rida Fatima Gilani, Mahnoor Fatima, Abdul Sattar Anjum, Sehrish Irshad   +5 more
wiley   +1 more source

Mutational Analysis of the LHX1 Gene in a French National Cohort of Patients with Mayer-Rokitansky-Küster-Hauser Syndrome

, 2015
International audienceObjective: Mayer-Rokitansky-Küster-Hauser syndrome (MRKH syndrome) is characterized by congenital aplasia of the uterus and the upper part of the vagina in women showing normal secondary sexual characteristics development and a ...
Folléa, N., Morcel, K, Voltzenlogel, M. C., Guerrier, D., Pasquier, L.   +4 more
core   +1 more source

Le syndrome de Mayer-Rokitansky-Küster-Hauser comme cause d'aménorrhée primaire: à propos d'un cas [PDF]

, 2021
Le syndrome de Mayer-Rokitansky-Küster-Hauser (MRKH) est une cause rare d´aménorrhée primaire. Il est défini par une aplasie congénitale de l´utérus et des deux tiers supérieurs du vagin chez des femmes présentant un développement normal des caractères ...
Meryem Edderai, Mohamed Abdellaoui, Jamal El Fenni   +2 more
core  

Neovaginal Diversion Colitis Successfully Treated With Mesalazine Suppositories: Endoscopic Documentation of Healing

Digestive Endoscopy, Volume 38, Issue 1, January 2026.
Shinichiro Kawatoko, Marimo Mori, Junji Umeno   +2 more
wiley   +1 more source

Sensibility of vagina reconstructed by McIndoe method in Mayer-Küster-Rokitansky-Hauser syndrome [PDF]

, 2008
Background/Aim. Congenital absence of vagina is a failure present in Mayer-Küster-Rokitansky-Hauser syndrome. Treatment of this anomaly includes nonoperative and operative procedures. McIndoe procedure uses split skin graft by Thiersch.
Panajotović Ljubomir, Garalejić Elijana, Svetlana Vesanovic, Ljubomir Panajotovic, Vesanović Svetlana, Elijana Garalejic   +5 more
core   +1 more source

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

, 2017
Mayer-Rokitansky-Küster-Hauser syndrome describes a vaginal and uterine agenesis, secondary to agenesis or hypoplasia of the Müllerian duct system.
Bailez, Marcela, Silva, Cristina Isabel Nogueira, Silva, Pedro Oliveira da, Reis, Isabel, Correia-Pinto, Jorge   +4 more
core   +1 more source

MAYER-ROKITANSKY-KUSTER-HAUSER SYNDROME (CLINICAL CASE)

Мать и дитя в Кузбассе, 2022
The Mayer-Rokitansky-Custer-Hauser syndrome (SMRCX) is a violation of the intrauterine development of the Pmuller ducts, leading to aplasia of the vagina and uterus. It is diagnosed in 1 out of 4500-5000 newborn girls.
Марина Анатольевна Ющенко, Алена Викторовна Робул, Светлана Ивановна Елгина, Вадим Гельевич Мозес, Елена Владимировна Рудаева, Анна Александровна Железная, Полина Никитична Мраморнова, Кира Борисовна Мозес   +7 more
doaj  

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  

Perfil clínico e sociodemográfico de um grupo de mulheres brasileiras com a Síndrome de Mayer-Rokitansky-Küster-Hauser

Os dados referem-se a características clínicas e sociodemográficas de um grupo de mulheres brasileiras com diagnóstico de Síndrome de Mayer-Rokitansky-Küster-Hauser assistidas pelo Instituo ...
Lídia Silveira dos Santos
core   +1 more source