Results 81 to 90 of about 1,143,195 (179)

Müllerian Duct Remnants on the Uterine Surface With Ovarian Serous Cystadenoma: A Case Report and Literature Review

Case Reports in Obstetrics and Gynecology, Volume 2026, Issue 1, 2026.
This report describes a case of a patient diagnosed with a residual Müllerian duct mass on the uterine surface at our hospital. Through analysis of this case and a review of the literature, we are aimed at reducing the risk of misdiagnosis and optimising treatment protocols for uterine cystic masses.
Wenxin Zhong, Xiuqing Lei, Shuangyang Qin, Yun Dai, Guangming Yang, Qi Bao, Dani Ejzenberg   +6 more
wiley   +1 more source

Mutations of cystic fibrosis transmembrane conductance regulator gene in patients with Mayer Rokitansky Kuster Hauser syndrome

مجله دانشگاه علوم پزشکی گرگان, 2014
Background and Objective: Mayer Rokitansky Kuster Hauser (MRKH) syndrome is characterized by Mullerian duct aplasia in an XX individual with female phenotype presenting primary amenorrhea at adolescence.
Asadi F, Hashemian Naeini ES
doaj  

Innovation in Vaginoplasty: Integration of a Silicone Tissue Expander Prosthesis Into the McIndoe Technique—A Case Report

Case Reports in Obstetrics and Gynecology, Volume 2026, Issue 1, 2026.
Background and Aims Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome is a congenital condition marked by agenesis of the uterus and upper vagina in individuals with a normal female karyotype. Surgical reconstruction is often required to enable satisfactory sexual function.
Ivonne Jeannette Díaz-Yamal, Mario Andrés Rodríguez-Albarracín, Daniela Pinto, Luis Bermúdez, Ana María Heredia, Manvinder Singh   +5 more
wiley   +1 more source

Clinical features and management of women with Mayer-Rokitansky-Küster-Hauser syndrome in a Thai population [PDF]

Obstetrics & Gynecology Science
Objective This study aimed to describe the clinical features, associated extragenital anomalies, and management of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome in a Thai population.
Phawat Matemanosak, Krantarat Peeyananjarassri, Satit Klangsin, Saranya Wattanakumtornkul, Kriengsak Dhanaworavibul, Chainarong Choksuchat, Chatpavit Getpook   +6 more
doaj   +1 more source

Congenital glaucoma prevention program—Evaluation of patient knowledge and acceptance of genetic screening

Journal of Genetic Counseling, Volume 34, Issue 5, October 2025.
Abstract This cross‐sectional study evaluated the knowledge and understanding of basic genetic concepts, as well as the acceptance of screening and preventive measures, among 100 adult patients and/or parents of children with primary congenital glaucoma (PCG) at King Khalid Eye Specialist Hospital. The study population included 36 males and 64 females.
Areej Alizary, Abdulwahab AlTheeb, Syed Hameed, Bashaer Almadani, Shereen Abualkhair, Leyla Ali Aljasim   +5 more
wiley   +1 more source

Evaluation and management of cases of primary amenorrhoea with MRKH syndrome

Bangladesh Medical Journal Khulna, 2013
The Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome, the second most common cause of primary amenorrhoea usually remains undetected until puberty and is characterized by congenital aplasia or hypoplasia of the uterus and most of the vagina in women showing normal secondary sexual characteristics.
Badrunnesa Begum, Nasreen Akhter
openaire   +2 more sources

Recurrent microdeletion at 17q12 as a cause of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome: two case reports [PDF]

, 2009
Background Mayer-Rokitansky-Kuster-Hauser syndrome (MRKH) consists of congenital aplasia of the uterus and the upper part of vagina due to anomalous development of Müllerian ducts, either isolated or associated with other congenital malformations ...
Monica Miozzo, Luigi Fedele, A. Baban, M. T. Divizia, Laura Bernardini, Giada Frontino, L. Bernardini, Giancarlo Barbano, G. Frontino, Béna Frédérique, Dallapiccola Bruno, Frontino Giada, Cristina Gervasini, C.C.G. Gervasini, Bernardini Laura, S. Gimelli, A. Novelli, Anwar Baban, Antonio Novelli, F. Lalatta, F. Bena, C. Gervasini, Divizia Maria, Gervasini Cristina, Frédérique Béna, B. Dallapiccola, Lalatta Faustina, Carella Massimo, L. Fedele, Fedele Luigi, Novelli Antonio, Bruno Dallapiccola, Massimo Carella, Faustina Lalatta, Baban Anwar, Miozzo Monica, M. Carella, Maria Divizia, M.R. Miozzo, Barbano Giancarlo, Stefania Gimelli, Gimelli Stefania, G. Barbano   +42 more
core   +1 more source

A rare form of Mayer-Rokitansky-Küster-Hauser syndrome: Case report and review of literature

Case Reports in Women's Health, 2019
Introduction: Primary amenorrhea is failure to reach menarche. Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is the second most common cause of primary amenorrhea, after gonadal dysgenesis.
Omran Al Dandan, Ali Hassan, Amna Alsaihati, Lujain Aljawad, Fathiya Almejhim   +4 more
doaj   +1 more source

Aging‐Associated Vacuolation of Multi‐Ciliated Cells in the Distal Mouse Oviduct Reflects Unique Cell Identity and Luminal Microenvironment

Aging Cell, Volume 24, Issue 7, July 2025.
Multi‐ciliated cells in the infundibulum and ampulla (INF/AMP) epithelium are vacuolated in aging. Unique cellular susceptibility of the INF/AMP epithelial population and aging‐associated decline in ovarian artery circulation, which supports the ovary and INF/AMP, contribute to this region‐specific vacuolation phenotype, as a consequence of a mildly ...
Keerthana Harwalkar, Nobuko Yamanaka, Alain S. Pacis, Selina Zhao, Katie Teng, Warwick Pitman, Mitaali Taskar, Vera Lynn, Alex Frances Thornton, Matthew J. Ford, Yojiro Yamanaka   +10 more
wiley   +1 more source

A rare case of 46,XX gonadal dysgenesis and Mayer-Rokitansky-Kuster-Hauser syndrome

Journal of Human Reproductive Sciences, 2016
46,XX gonadal dysgenesis is a rare genetically heterogeneous disorder characterized by underdeveloped ovaries with consequent, impuberism, primary amenorrhea, and hypergonadotropic hypogonadism. Mullerian agenesis or Mayer-Rokitansky-Kuster-Hauser (MRKH)
Sriharibabu Manne, C H Veeraabhinav, Mounica Jetti, Yalamanchali Himabindu, Kiranmai Donthu, Mutyalarayudu Badireddy   +5 more
doaj   +1 more source