[PDF] springer.com

Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: a comprehensive update

MK Herlin, MB Petersen, M Brännström - Orphanet Journal of Rare …, 2020 - Springer
Abstract Background Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome, also referred to
as Müllerian aplasia, is a congenital disorder characterized by aplasia of the uterus and …
被引用次数：243 相关文章 所有 19 个版本

Genetics of mayer–rokitansky–küster–hauser (MRKH) syndrome

L Fontana, B Gentilin, L Fedele, C Gervasini… - Clinical …, 2017 - Wiley Online Library
Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome, also referred to as Müllerian
agenesis, is the second most common cause of primary amenorrhea. It is characterized by …
被引用次数：206 相关文章 所有 7 个版本
[PDF] springer.com

Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome

K Morcel, L Camborieux… - Orphanet journal of rare …, 2007 - Springer
Abstract The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is characterized by
congenital aplasia of the uterus and the upper part (2/3) of the vagina in women showing …
被引用次数：567 相关文章 所有 21 个版本

Typical and atypical associated findings in a group of 346 patients with Mayer-Rokitansky-Kuester-Hauser syndrome

K Rall, S Eisenbeis, V Henninger, M Henes… - Journal of pediatric and …, 2015 - Elsevier
Abstract Study Objective The Mayer-Rokitansky-Kuester-Hauser (MRKH) syndrome is
characterized by vaginal and uterine aplasia in a 46, XX individual. Multiple abnormalities …
被引用次数：107 相关文章 所有 8 个版本
[PDF] springer.com

The Mayer-Rokitansky-Küster-Hauser syndrome (congenital absence of uterus and vagina)–phenotypic manifestations and genetic approaches

D Guerrier, T Mouchel, L Pasquier, I Pellerin - Journal of negative results …, 2006 - Springer
Abstract The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome affects at least 1 out of
4500 women and has for a long time been considered as a sporadic anomaly. Congenital …
被引用次数：249 相关文章 所有 17 个版本
[PDF] researchgate.net

Familial occurrence of Mayer–Rokitansky–Küster–Hauser syndrome: a case report and review of the literature

M Herlin, AT Højland… - American Journal of …, 2014 - Wiley Online Library
Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome is a congenital disorder of still
unknown etiology, characterized by uterovaginal agenesis and can be associated with …
被引用次数：93 相关文章 所有 7 个版本
[PDF] academia.edu

Mayer–Rokitansky–Kuster–Hauser syndrome: recent clinical and genetic findings

C Sultan, A Biason-Lauber… - Gynecological …, 2009 - Taylor & Francis
Mayer–Rokitansky–Kuster–Hauser (MRKH) syndrome is characterized by Müllerian duct
aplasia in an XX individual with female phenotype presenting primary amenorrhea at …
被引用次数：205 相关文章 所有 7 个版本

The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: clinical description and genetics

K Morcel, D Guerrier, T Watrin, I Pellerin… - … obstetrique et biologie …, 2008 - europepmc.org
The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is characterized by congenital
aplasia of the uterus and the upper part (two-third) of the vagina. It may be isolated (type I) or …
被引用次数：108 相关文章 所有 2 个版本
[PDF] oup.com

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

M Herlin, AMB Bjørn, M Rasmussen, B Trolle… - Human …, 2016 - academic.oup.com
STUDY QUESTION What is the prevalence of Mayer–Rokitansky–Küster–Hauser (MRKH)
syndrome? SUMMARY ANSWER The prevalence of MRKH syndrome in Denmark is 1 in …
被引用次数：163 相关文章 所有 8 个版本
[HTML] rbmojournal.com

The reproductive potential of patients with Mayer–Rokitansky–Küster–Hauser syndrome using gestational surrogacy: a systematic review

S Friedler, L Grin, G Liberti, B Saar-Ryss… - Reproductive …, 2016 - Elsevier
Abstract Women with Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome may reproduce
after uterine transplantation or IVF using a gestational surrogate. As uterine transplantation …
被引用次数：74 相关文章 所有 8 个版本