Results 71 to 80 of about 1,398,641 (158)

Advanced‐Stage Gonadal Dysgerminoma in a Patient With a Previous Diagnosis of Familial Swyer Syndrome: A Very Rare Genetic Entity

Case Reports in Medicine, Volume 2026, Issue 1, 2026.
Introduction Swyer syndrome is a genetic abnormality characterized by a 46,XY karyotype in a phenotypically female individual. Affected individuals typically have average or tall stature, unambiguous genitalia at birth, the presence of Müllerian structures, and bilateral streak gonads.
Süleyman Cemil Oğlak, Nilgün Söğütçü, Sedat Akgöl, Özgür Adıgüzel, Hümeyra Elif Ateş Eminoğlu, Gizem Güzel, Veysi Balcı, Emine Acar, Abdullah Acar, Fuat Bozan, Aneek Das Bhowmik   +10 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  

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

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

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

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  

Mayer-Rokitansky-Kuster-Hauser syndrome (MRKHS), a rare cause of primary amenorrhoea: three case reports

Sri Lanka Journal of Diabetes Endocrinology and Metabolism, 2017
Primary amenorrhoea is one of the common reproductive disorders affecting females and it could be due to may causes including structural, functional and endocrine abnormalities.
D. Karuppiah, S. Dilakkumar
doaj   +1 more source

A rare case of Mayer-Rokitansky-Kuster-Hauser syndrome with multiple leiomyomas in hypoplastic uterus

Journal of Human Reproductive Sciences, 2015
Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is a rare disorder described as aplasia or hypoplasia of uterus and vagina due to an early arrest in development of mullerian ducts.
Maithili Mandar Kulkarni, Sanjay D Deshmukh, Kishor Hol, Neha Nene   +3 more
doaj   +1 more source

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