Results 51 to 60 of about 1,143,195 (179)
Anxiety symptoms in patients with Mayer-Rokitansky-Küster-Hauser syndrome: a cross-sectional study
Chinese Medical Journal, 2020 . Background:. As a congenital malformation that results in infertility and an inability to have vaginal intercourse, Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome places a considerable psychological burden on patients, which results in anxiety symptoms.
Shuang Song +7 more
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Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: a comprehensive update [PDF]
Yearbook of Paediatric Endocrinology, 2021 Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome, also referred to as Mullerian aplasia, is a congenital disorder characterized by aplasia of the uterus and upper part of the vagina in females with normal secondary sex characteristics and a normal female karyotype (46,XX).
Herlin MK, Petersen MB, Brannstrom M
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Sociocultural Effects on Women with MRKH Syndrome
, 2021 : Mayer-Rokitansky-Küster-Hauser syndrome (MRKH) is a congenital disease that affects the female reproductive organs, causing them to be either malformed or completely absent.
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Magnetic Resonance Imaging in Mayer-Rokitansky-Kuster-Hauser Syndrome: A Retrospective Study [PDF]
International Journal of Anatomy Radiology and Surgery, 2020 Introduction: Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is a congenital anomaly in female genital tract owing to irregular embryonic development of para-mesonephric ducts and thus leads to uterine and proximal vagina aplasia or hypoplasia.
VELICHETI SANDEEP +4 more
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Orphanet Journal of Rare Diseases, 2020 Background Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is a rare congenital disease characterized by uterovaginal agenesis. The diagnosis of MRKH syndrome generally leads to considerable emotional burdens on patients.
Na Chen +6 more
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Clinical Genetics, EarlyView.Genetic causes of Müllerian aplasia remain largely unknown. We report the first molecularly confirmed case of Coffin–Siris syndrome 3 caused by a de novo SMARCB1 variant presenting with Müllerian aplasia, supporting a potential association between BAF complex dysfunction and abnormal Müllerian duct development. Created in BioRender. Herlin, M. K. (2026)
Anneli C. S. Bolund +5 more
wiley +1 more source
Acta Obstetricia et Gynecologica Scandinavica, Volume 105, Issue 9, Page 1810-1822, September 2026.Overall, 21 patients with uterine, cervical, and vaginal aplasia were treated successfully with neovagina formation. In 6 out of 8 patients, with obstructed uterine cavity, anastomosis was successful; one underwent hysterectomy and one elective hemi‐hysterectomy.
Grigoris F. Grimbizis +5 more
wiley +1 more source
Modern competency‐based teaching of human sexual development
Anatomical Sciences Education, Volume 19, Issue 7, Page 1086-1096, July 2026.Abstract Embryology is an integral part of anatomy and a key subject in basic medical education. The development of the sexual tract, which is closely associated with the formation of the urinary tract and the organs of continence, is particularly complex and relevant for many medical disciplines.
Elisabeth Eppler +2 more
wiley +1 more source
Patient with Mayer-Rokitansky-Kuster-Hauser syndrome (MRKH) who Underwent Laparoscopic Davydov-Moore vaginoplasty [PDF]
, 2020 The Mayer-Rokitansky-Kuster-Hauser syndrome (MRKH) constitutes the second most common cause of primary amenorrhea, after gonadal dysgenesis. It is a congenital absence of the vagina with variable uterine development, which is a result of Mullerian duct ...
Zmaczyński, Andrzej +7 more
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Taiwanese Journal of Obstetrics & GynecologyObjective: Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is a rare congenital disorder that results in vaginal agenesis. Lee's neovaginoplasty is a novel surgery for reconstructing the vagina.
Le Tien Hsu +4 more
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