Mayer-Rokitansky-Künster-Hauser syndrome due to 2q12.1q14.1 deletion: PAX8 the causing gene?
Sign Up to like & getrecommendations! Published in 2019 at "European journal of medical genetics"
DOI: 10.1016/j.ejmg.2019.103812
Abstract: Mayer-Rokitansky-Küster-Hauser syndrome (MRKH) is a rare malformative disorder, characterized by congenital aplasia of the uterus and the upper two thirds of the vagina (MIM #277000). For a majority of patients, the disorder remained without identified… read more here.
Keywords: pax8; 2q12 1q14; hauser syndrome; mayer rokitansky ... See more keywords
Laparoscopic Creation of a Neovagina in Mayer-Rokitansky-Küster-Hauser Syndrome
Sign Up to like & getrecommendations! Published in 2019 at "Journal of Minimally Invasive Gynecology"
DOI: 10.1016/j.jmig.2019.09.741
Abstract: Video Objective To show the step by step procedure of a neovagina creation in Mayer-Rokitansky-Kuster-Hauser Syndrome. Setting 22-year-old patient with primary amenorrhea, normal feminine phenotype development and vaginal agenesis on clinical examination. Pelvic ultrasound noted… read more here.
Keywords: laparoscopic; hauser syndrome; mayer rokitansky; creation ... See more keywords
Multiorgan system structural malformations associated with Mayer-Rokitansky-Küster-Hauser Syndrome (MRKHS) type 2: avoiding pitfalls in diagnosis, counseling and treatment
Sign Up to like & getrecommendations! Published in 2018 at "BMJ Case Reports"
DOI: 10.1136/bcr-2018-225977
Abstract: An 18-year-old virginal woman was referred to the reproductive endocrinology clinic with primary amenorrhoea and secondary sexual development in the absence of pelvic pain. Additionally, she had significant congenital sensorineural hearing loss, autism, bipolar disorder… read more here.
Keywords: ster hauser; diagnosis; rokitansky ster; hauser syndrome ... See more keywords
Adenomyosis in a uterine horn of a patient with Mayer-Rokitansky-Kuster-Hauser syndrome
Sign Up to like & getrecommendations! Published in 2022 at "BMJ Case Reports"
DOI: 10.1136/bcr-2021-244127
Abstract: A 37-year-old woman with a previous diagnosis of Mayer-Rokitansky-Kuster-Hauser syndrome at 18 years of age was referred from a primary healthcare physician to a gynaecology appointment in our centre. She presented with a 2-year worsening… read more here.
Keywords: horn patient; mayer rokitansky; kuster hauser; rokitansky kuster ... See more keywords
Vaginoplasty with Oxidized Cellulose in Mayer–Rokitansky–Küster–Hauser Syndrome
Sign Up to like & getrecommendations! Published in 2021 at "Journal of Indian Association of Pediatric Surgeons"
DOI: 10.4103/jiaps.jiaps_76_20
Abstract: Mayer–Rokitansky–Küster–Hauser syndrome (MRKHS) is the major cause of vaginal agenesis. Vaginoplasty with oxidized cellulose has been used by gynecologists as a surgical option in vaginal agenesis; however, it is not very widespread among pediatric surgeons.… read more here.
Keywords: mayer rokitansky; ster hauser; oxidized cellulose; vaginoplasty oxidized ... See more keywords
Methods for neovagina creation in women with Mayer-Rokitansky-Küster-Hauser syndrome for subsequent uterus transplantation.
Sign Up to like & getrecommendations! Published in 2021 at "Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia"
DOI: 10.5507/bp.2021.049
Abstract: Mayer-Rokitansky-Küster-Hauser syndrome is a rare female congenital anomaly that presents with an inability to have coital sexual intercourse and absolute uterine factor infertility. Both surgical and nonsurgical approaches have been described for the treatment of… read more here.
Keywords: ster hauser; rokitansky ster; hauser syndrome; transplantation ... See more keywords