Results 41 to 50 of about 1,143,195 (179)
Human Genomics, 2022 Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome, also known as Müllerian agenesis, is characterized by uterovaginal aplasia in an otherwise phenotypically normal female with a normal 46,XX karyotype.
Chunfang Chu +8 more
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Fertility options in Mayer-Rokitansky-Küster-Hauser syndrome
Clinical and Experimental Obstetrics & Gynecology, 2021 Background: The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is the most common cause of uterine aplasia, with a worldwide frequency of 1 in 4500 females.
Francesco Fedele +3 more
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Clinical efficacy of laparoscopic peritoneal vaginoplasty in the treatment of MRKH syndrome
生物医学转化Objective To investigate the clinical efficacy of laparoscopic peritoneal vaginoplasty (Luohu Type II) in the treatment of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome. Methods A retrospective analysis was conducted on the clinical data of 221 patients with MRKH syndrome treated at the Third Affiliated Hospital of Shenzhen University (Shenzhen Luohu ...
Qin Chenglu +9 more
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Type 2 Variant of Mayer-Rokitansky-Kuster-Hauser Syndrome: A Case Report [PDF]
Journal of Clinical and Diagnostic ResearchMayer-Rokitansky-Küster-Hauser (MRKH) syndrome is an autosomal dominant condition that may co-occur with cardiac, renal, and skeletal abnormalities. It affects females causing utero-vaginal agenesis.
Sri Divya Cherukuri +4 more
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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 +6 more
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MRKH SYNDROME: KEY ROLE OF COUNSELING
Journal of Evolution of Medical and Dental Sciences, 2014 Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is a congenital malformation of vertical fusion defect of mullerian system characterized by an absence of the vagina associated with a variable abnormality of the uterus and the urinary tract but functional ovaries. We are reporting 21 years primary ammenorrhea case.
Yelikar K A +4 more
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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 +3 more
doaj +1 more source
In utero phthalate effects in the female rat: A model for MRKH syndrome [PDF]
Toxicology Letters, 2013 Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is characterized by uterine and vaginal canal aplasia in normal karyotype human females and is a syndrome with poorly defined etiology. Reproductive toxicity of phthalate esters (PEs) occurs in rat offspring exposed in utero, a phenomenon that is better studied in male offspring than females.
Hannas, Bethany R. +3 more
openaire +2 more sources
Avoiding Re-Traumatization and Healthcare Avoidance in Women with MRKH Syndrome
, 2023 Mayer-Rokitansky-Küster-Hauser Syndrome (MRKH) is a congenital disorder among biological females that is characterized by the absence or underdevelopment of the uterus, vagina, and cervix (Laggari et al., 2009).
Podolin, Danielle
core +2 more sources
, 2009 Background: Uterovaginal agenesis (Mayer-Rokitansky-Kuster-Hauser Syndrome; MRKH) is a congenital nonformation of the vagina and the uterus, but with normal ovaries.
Edmonds, D. Keith +2 more
core +5 more sources