Results 91 to 100 of about 1,400,939 (196)

Mayer-Rokitansky-Kuster-Hauser syndrome associated with unilateral gonadal agenesis - A case report

, 2020
BACKGROUND: Mayer-Rokitansky-Kuster-Hauser syndrome is the second most frequent cause of primary amenorrhea, with a reported incidence of 0.002%. Patients have a normal karyotype and usually normal ovaries.
Kose, SA, Ozkaya, O, Sezik, Mekin, Kaya, H   +3 more
core  

HEARING-LOSS AND THE MAYER-ROKITANSKY-KUSTER-HAUSER SYNDROME

, 1994
The hearing of 51 female patients with the Mayer-Rokitansky-Kuster-Hauser syndrome was examined using otoscopy and standard audiometry. A unilateral or bilateral hearing loss of more than 15 dB Fletcher index was found in 13 of 51 (25.5%).
DIKKERS, FG, STRUBBE, EH, CREMERS, CWRJ, WILLEMSEN, WNP   +3 more
core   +1 more source

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

Reproductive Biology and Endocrinology, 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 ...
Oppelt Patricia G, Lermann Johannes, Strick Reiner, Dittrich Ralf, Strissel Pamela, Rettig Ingo, Schulze Christine, Renner Stefan P, Beckmann Matthias W, Brucker Sara, Rall Katharina, Mueller Andreas   +11 more
doaj   +1 more source

Rare case of leiomyoma in Mayer-Rokitansky-Kuster-Hauser syndrome [PDF]

, 2017
Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is a cause for primary amenorrhea. It is characterized by the presence of XX karyotype, normal ovarian function and blind vaginal pouch.
Bhuyar, Sonal A.
core  

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 (a clinical case)

, 2017
Congenital aplasia of the uterus and vagina occurs from 1 in 5000 to 1 in 20000 among newborn girls. Clinical case. A 16-year-old patient A. was admitted to the Regional Children’s Clinical Hospital No.1 of the Department of Obstetrics, Gynecology and ...
Pilipenko, Natalia, Romanova, Natalia
core   +1 more source

Mayer–Rokitansky–Kuster–Hauser syndrome: Syndrome of Mullerian agenesis – A report of two cases

, 2017
The Mayer–Rokitansky–Kuster–Hauser syndrome (MRKH syndrome), simply called Rokitansky syndrome or vaginal aplasia of the uterus, is a congenital condition that is characterized by the absence of the uterus and vagina, but ovaries are present and the ...
Sushma Yalavarthi, Varsha A Jadhav, S Susheel Kumar, M Pavani   +3 more
core   +1 more source

KIDNEY ON MAYER-ROKITANSKY-KÜSTER-HAUSER SYNDROME [PDF]

, 2014
The Mayer-Rokitansky-Küster-Hauser syndrome (MRKH) is a rare disorder characterized by congenital absence of upper part of the vagina and the absence or atresia of the uterus. The prevalence has been reported as one in 4000-5000 female births.
Breda, Giovanni Luis, Ascenço, Henrique Guesser, Carvalho, Maurício   +2 more
core   +1 more source

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

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