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Mayer-Rokitansky-Küster-Hauser syndrome


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'Mayer-Rokitansky-Küster-Hauser syndrome' can also refer to...

Mayer-Rokitansky-Küster-Hauser syndrome

Mayer–Rokitansky–Küster–Hauser syndrome

Mayer-Rokitansky-Küster-Hauser syndrome (1795–1868)

Frame shift mutation of LHX1 is associated with Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome

Simplifying ovulation induction for surrogacy in women with Mayer-Rokitansky-Kuster-Hauser syndrome.

Higher incidence of linked malformations in siblings of Mayer–Rokitansky–Küster–Hauser-syndrome patients

Normalization of the vagina by dilator treatment alone in Complete Androgen Insensitivity Syndrome and Mayer-Rokitansky-Kuster-Hauser Syndrome

Vaginal agenesis (Mayer-Rokitansky-Kuster-Hauser Syndrome) associated with the N314D mutation of galactose-1-phosphate uridyl transferase (GALT)

Surrogate in vitro fertilization outcome in typical and atypical forms of Mayer–Rokitansky–Küster–Hauser syndrome

Use of artificial dermis and recombinant basic fibroblast growth factor for creating a neovagina in a patient with Mayer–Rokitansky–Küster–Hauser syndrome

Laparoscopic extirpation of an aplastic ectopic uterus in a patient with Mayer-Rokitansky-Küster-Hauser syndrome.

WNT4 deficiency—a clinical phenotype distinct from the classic Mayer–Rokitansky–Kuster–Hauser syndrome: A Case Report

Vaginoplasty using autologous in vitro cultured vaginal tissue in a patient with Mayer–von-Rokitansky–Küster–Hauser syndrome

Prevalence and patient characteristics of Mayer–Rokitansky–Küster–Hauser syndrome: a nationwide registry-based study

Mayer–von Rokitansky–Küster–Hauser syndrome in association with a hitherto undescribed variant of the Holt–Oram syndrome with an aorto‐pulmonary window

Concurrent exome-targeted next-generation sequencing and single nucleotide polymorphism array to identify the causative genetic aberrations of isolated Mayer–Rokitansky–Küster–Hauser syndrome

A randomized controlled trial of a cognitive-behavioural group intervention versus waiting-list control for women with uterovaginal agenesis (Mayer–Rokitansky–Küster–Hauser syndrome: MRKH)

 

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(Rokitansky-Küster-Hauser syndrome, Müllerian agenesis) congenital absence of the uterus and upper part of the vagina due to failure of development of the Müllerian duct. It may be associated with skeletal, renal, and auditory abnormalities, but usually presents with amenorrhoea in a patient with otherwise normal secondary sexual characteristics. There is a multidisciplinary approach to treatment, with psychological support, counselling, discussion of creation of a ‘neovagina’ with gradual use of vaginal dilators, and/or surgical vaginal reconstruction. Surrogacy is the only option for childbearing, although oocyte donation from the mother to a surrogate can be discussed. K. W. Mayer (1795–1868), German gynaecologist; K. von Rokitansky (1804–78), Austrian pathologist; H. Küster and G. A. Hauser (20th century), German gynaecologists

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