Results 21 to 30 of about 1,400,939 (196)

Long-Term Psychosocial Outcomes in Japanese Mayer-Rokitansky-Küster-Hauser Syndrome: A Single-Center Study. [PDF]

J Obstet Gynaecol Res
ABSTRACT Aim Vaginal creation enables sexual intercourse in patients with Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome. However, long‐term psychosocial outcomes, particularly in Japanese patients, remain underreported. This study aimed to explore the long‐term psychosocial outcomes associated with different choices of vaginal creation in patients ...
Okunomiya A, Tsuyuki K, Ohsuga T, Ohara T, Yanai A, Mizuno R, Yamanoi K, Egawa M, Mandai M.   +8 more
europepmc   +2 more sources

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   +1 more source

Vaginal endometriosis following uterine transplantation in a patient with Mayer-Rokitansky-Küster-Hauser syndrome: A unique case report. [PDF]

Int J Gynaecol Obstet
International Journal of Gynecology &Obstetrics, Volume 172, Issue 3, Page 1794-1795, March 2026.
Moravcova J, Chmel R, Maluskova J, Sticova E.   +3 more
europepmc   +2 more sources

Hollow vaginal stent for a case of Mayer-Rokitansky-Kuster-Hauser syndrome: a case report

The Pan African Medical Journal, 2021
Congenital vaginal agenesis is a common condition with an instance of 1 in 5000 females. It is usually associated with Mayer-Rokitansky-Kuster Hauser syndrome. Such anomalies have a high impact on the physiology and psychology of patients.
Sharayu Vinod Nimonkar, Vikram Murlidhar Belkhode   +1 more
doaj   +1 more source

Mayer – Rokitansky – Kuster – Hauser syndrome

Journal of Obstetrics and Gynaecology, 2006
It is becoming increasingly common to identify complex early gestational fetal abnormalities through post-mortem examination, and also increasingly difficult to characterise these complex occurrenc...
M, Chandiramani, C A, Gardiner, C J H, Padfield, S E, Ikhena   +3 more
openaire   +3 more sources

Mayer-Rokitansky-Kuster-Hauser Syndrome

, 2016
Mayer-Rokitansky-Kuster-Hauser Syndrome is a congenital disorder of the female reproductive tract due to impaired Müllerian duct development. There are three known categorical presentations: isolated, atypical, and MURCS association.
Shy, Hannah Marie
core   +4 more sources

Rare association of Turner syndrome and Mayer-Rokitansky-Kuster Hauser syndrome [PDF]

, 2022
Turner syndrome and Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is a rare association. The incidences of Turner and MRKH syndromes are estimated at 1/2000 and 1/4500 female births respectively.
Ndiade, Amadou, Sy, Mama, Dia, Sérigne A. M., Thiam, Mbaye   +3 more
core   +1 more source

Mayer-Rokitansky-Kuster-Hauser Syndrome.

Journal of Ayub Medical College, Abbottabad : JAMC, 2014
Mayer-Rokitansky-Küster-Hauser Syndrome is a congenital malformation in which there is failure of the Müllerian ducts to develop resulting in absent uterus and fallopian tubes and variable malformations of the vagina. Ultrasonography reveals absence of uterus with normally visualised ovaries.
Ruqqayia, Adil, Adil, Qayyum
openaire   +3 more sources

Mayer–Rokitansky–Küster–Hauser syndrome

Акушерство, гинекология и репродукция, 2023
The Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome is an instructive story not only from a historical but also a gnoseological perspective. The mechanisms of embryogenesis as well as multiple aspects for correction of this syndrome remain enigmatic and ...
R. T. Adamyan, A. K. Blbulyan, R. A. Abrahamyan, L. R. Abrahamyan, G. R. Abrahamyan, G. K. Ghardyan, D. A. Blbulyan   +6 more
doaj   +1 more source

Mayer-rokitansky-kuster-hauser syndrome with hyperprolactinemia

Saudi Medical Journal, 2008
Mayer-Rokitansky-Kuster-Hauser Syndrome in association with hyperprolactinemia is very rare. An 18-year-old, Saudi, single, virgin female was accompanied by her mother seeking medical advice regarding absent menses. She had normal breasts, normal axillary and pubic hair, normal vulva, urethra, and labial folds, however, the vagina was blind ...
Dania H, Al-Jaroudi, Ayda M, Nasser
openaire   +2 more sources