Results 11 to 20 of about 1,398,641 (158)

Coffin-Siris syndrome with Mayer-Rokitansky-Küster-Hauser syndrome: a case report [PDF]

Journal of Medical Case Reports, 2010
Introduction We report the case of an unusual association of Coffin-Siris syndrome with Mayer-Rokitansky-Küster-Hauser syndrome. This association has never previously been reported in the medical literature.
Shukla Umesh, Yadav Dinesh K, Goyal Deepak, Sethi Sidharth K   +3 more
doaj   +3 more sources

Thyroid carcinoma and primary amenorrhea due to Mayer-Rokitansky-Küster-Hauser syndrome: a case report [PDF]

Journal of Medical Case Reports, 2012
Introduction This case report describes an association between an exceptionally rare congenital anomaly and differentiated thyroid carcinoma. Mayer-Rokitansky-Küster-Hauser syndrome is characterized by vaginal aplasia associated with other Müllerian duct
Piciu Doina, Piciu Andra, Irimie Alexandru   +2 more
doaj   +3 more sources

A case of Mayer-Rokitansky-Küster-Hauser syndrome in a low-resource tertiary hospital in Douala, Cameroon

SAGE Open Medical Case Reports, 2019
The Mayer-Rokitansky-Küster-Hauser syndrome is the congenital absence or underdevelopment of the uterus and vagina even though the external genitalia, ovaries and ovarian function are normal. This condition is uncommon in Cameroon. A 23-year-old woman of
Thomas Obinchemti Egbe, Fidelia Mbi Kobenge, Metogo Mbengono Junette Arlette, Jacque-Ernest Nyemb, Robinson Enow Mbu   +4 more
doaj   +2 more sources

Mayer Rokitansky Kuster Hauser Syndrome [PDF]

Andalas Obstetrics and Gynecology Journal, 2023
Mayer Rokitansky Küster Hauser syndrome (MRKH) is a syndrome characterized by uterine, cervix, and the two third of upper vagina aplasia which is the cause of incomplete development of the Müllerian duct.
Arga Kafi Perdana Kusuma, Bobby Indra Utama   +1 more
doaj   +2 more sources

A Case of Iron Overload–Associated Hypogonadism and Mayer–Rokitansky–Küster–Hauser Syndrome in a Patient With Thalassemia

Annals of Internal Medicine: Clinical Cases
We report a rare case of a 22-year-old woman with transfusion-dependent beta-thalassemia major who presented with primary amenorrhea. Work-up revealed dual etiologies: hypogonadotropic hypogonadism attributable to pituitary iron overload and müllerian ...
Ravi Krishnegowda, Nagaraja Kamath, Naveen Kumar, Rishika Das, Aditya Chandrashekar   +4 more
doaj   +2 more sources

SINDROME DE MAYER-ROKITANSKY-KÜSTER-HAUSER: EXPERIENCIA CON VAGINOPLASTIA POR TRACCION LAPAROSCOPICA

Revista Chilena de Obstetricia y Ginecología, 2003
Se presenta un caso clínico de síndrome de Mayer-Rokitansky-Küster-Hauser, tratado con vaginoplastia laparoscópicaA clinical case of Mayer-Rokitansky syndrome is presented, treated by vaginal plastic surgery via laparoscopic with ...
Cristián Pomes C., Nicanor Barrena M.
doaj   +2 more sources

Island Singapore Flap Vaginoplasty of Two Adult Cases of Mayer– Rokitansky–Küster–Hauser Syndrome Type I [PDF]

The Annals of African Surgery, 2019
Mayer–Rokitansky–Küster–Hauser Syndrome Type I is an emotionally distressful rare condition that limits normal sexual functioning and relationships. First described in 1989 by Wee and Joseph, the neurovascular island pudendal thigh flap (Singapore flap ...
Alex Okello Wamalwa, Stanely Ominde Khainga   +1 more
doaj   +2 more sources

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

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   +2 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

Data for: Detection of De novo Genetic Variants in Mayer-Rokitansky-Küster-Hauser syndrome by Whole Genome Sequencing

, 2019
Data for: Detection of De novo Genetic Variants in Mayer-Rokitansky-Küster-Hauser syndrome by Whole Genome ...
hongxin pan (7184819)
core   +3 more sources