Unraveling the Genetic Mysteries of Müllerian Anomalies: Research Approaches and Clinical Significance. [PDF]
Clin GenetThis review primarily summarizes the genetic defects in Müllerian anomalies, the tools used to validate these genetic defects, and the future clinical significance of identifying the precise genetic etiology of Müllerian anomalies. ABSTRACT Müllerian anomalies are a collection of heterogeneous anatomical disorders of the female genital tract that ...
Li J, Hou X, Wang X, Li J, Li L, Ma X.
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Vaginal agenesis (Mayer-Rokitansky-Kuster-Hauser syndrome) presenting with exertional dyspnoea, fatigue and intermittent palpitations [PDF]
European Journal of Case Reports in Internal MedicineIntroduction: Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome represents a spectrum of Müllerian duct anomalies. MRKH type I involves isolated agenesis of the uterus and vagina, while MRKH type II involves extra-genital defects most commonly affecting the
Priti Dave +4 more
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Mayer–Rokitansky–Kuster–Hauser Syndrome: From Radiological Diagnosis to Further Challenges—Review and Update [PDF]
DiagnosticsMayer–Rokitansky–Küster–Hauser (MRKH) syndrome encompasses a range of Müllerian duct anomalies characterized by congenital absence of the uterus and the upper two-thirds of the vagina in young women who otherwise exhibit normal endocrine function and a ...
Calin Schiau +5 more
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Gynecological Endocrinology, 2015 Infertility has previously been considered as an inevitable consequence of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome. With modern assisted reproductive technology (ART) techniques becoming increasingly accessible, MRKH women have the opportunity for their own genetic offspring. The availability of such technology, however, increases the importance
Craig Jefferies, Lynsey M Cree
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Spectrum of MRI Appearance of Mayer-Rokitansky-Kuster-Hauser (MRKH) Syndrome in Primary Amenorrhea Patients [PDF]
Journal of Clinical and Diagnostic Research, 2017 Introduction: Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is a malformation in female genital tract due to interrupted embryonic development of para-mesonephric ducts leading to uterine and proximal vagina aplasia or hypoplasia. Aim: To analyse the
Deb Kumar Boruah +7 more
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A rare case of multiple leiomyomas on rudimentary uterus in a woman with Mayer Rokitansky Kuster Hauser (MRKH) syndrome: A challenging diagnosis and laparoscopic approach [PDF]
International Journal of Surgery Case Reports, 2021 Achmad Kemal Harzif, Sonia Priyadarshini
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Giant hysteromyoma after vaginoplasty in a woman with Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: case report and review of the literature [PDF]
Journal of International Medical Research, 2021 Fei Wang
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Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome - a review
Indian Journal of Urology, 2002 Purpose: Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is a congenital malformation characterized by an absence of the vagina associated with a variable abnormality of the uterus and the urinary tract butfunc-tional ovaries. We review the embryological, endocrino-logical, clinical, diagnostic, psychosocial and therapeutic features of this syndrome ...
N P Gupta, M S Ansari
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Experiences of Pelvic and Generalized Persistent Pain Syndromes in MRKH: A Scoping Review
Journal of Pediatric and Adolescent GynecologyMayer-Rokitansky-Küster-Hauser (MRKH) syndrome is characterized by the congenital absence of the uterus and vagina, sometimes with associated extragenital anomalies. Currently, there is limited literature on pelvic pain and comorbid pain syndromes in people with MRKH.
Gaikaiwari, RU +4 more
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Recurrent human 16p11.2 microdeletions in type I Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome patients in Chinese Han population [PDF]
Molecular Genetics & Genomic MedicineZhenwei Xie, Han Liu, Daizhan Zhou
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