Results 81 to 90 of about 1,400,939 (196)

How do women with Rokitansky syndrome and healthcare professionals reflect on the provision of uterine transplantation? Insights from an interview study in France, Norway, and Sweden

Acta Obstetricia et Gynecologica Scandinavica
Introduction Uterine transplantation is currently intended for women with absolute uterine infertility. Since proof of the concept in 2014, many countries have started research programs and clinical activities.
Isis Carton, Ludivine Dion, Vincent Lavoué, Bjorn Morten Hofmann   +3 more
doaj   +1 more source

Ileum neovaginoplasty for Mayer–Rokitansky–Küster–Hauser: Review and case series

African Journal of Urology, 2017
Objective: To review treatment modalities of Mayer–Rokitansky–Küster–Hauser syndrome, and to present further evidence on the successful use of ileum segment as an additional procedure for the creation of a neovagina.
L. Al-Mehaisen, Z. Amarin, O. Bani Hani, F. Ziad, O. Al-Kuran   +4 more
doaj   +1 more source

Methods for neovagina creation in women with Mayer-Rokitansky-Küster-Hauser syndrome for subsequent uterus transplantation

Biomedical Papers, 2021
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.
Roman Chmel, Zlatko Pastor, Marta Novackova, Nikoleta Chubanovova, Roman Chmel   +4 more
doaj  

SINDROME DE MAYER-ROKITANSKY-KÜSTER-HAUSER: EXPERIENCIA CON VAGINOPLASTIA POR TRACCION LAPAROSCOPICA

Revista Chilena de Obstetricia y Ginecología, 2003
Se presenta un caso clínico de síndrome de Mayer-Rokitansky-Küster-Hauser, tratado con vaginoplastia laparoscópicaA clinical case of Mayer-Rokitansky syndrome is presented, treated by vaginal plastic surgery via laparoscopic with ...
Cristián Pomes C., Nicanor Barrena M.
doaj  

Vaginoplasty with Amnion Graft: Management of Mayer-Rokitansky-Kuster-Hauser Syndrome

Journal of Nepal Health Research Council
Mayer-Rokitansky-Kuster-Hauser syndrome also known as mullerian agenesis is a rare congenital condition in which there is absence of uterus along with upper vagina.
Srijana Bhandari, Ganesh Dangal, Aruna Karki, Hema Pradhan, Ranjana Shrestha, Kabin Bhattachan, Kenusha Devi Tiwari, Sonu Bharati, Sunita Maharjan   +8 more
doaj   +1 more source

Toward Next‐Generation Teratology: Understanding Developmental Vulnerability Through Evolutionary and Comparative Genomics

Congenital Anomalies, Volume 66, Issue 1, January/February 2026.
ABSTRACT Teratology, the study of congenital anomalies, has developed from a descriptive discipline into a mechanistic science focused on the proximate causes of developmental defects, meaning how such anomalies arise during development. However, a comprehensive understanding requires not only this mechanistic insight but also an evolutionary ...
Tetsuo Kon
wiley   +1 more source

Surgical and functional outcome of sigmoid colon-vaginoplasty in Mayer-Rokitansky-Kuster-Hauser syndrome [PDF]

, 2017
Background: The objective of this study is to report our experience with sigmoid vaginoplasty in adolescent female patients of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome with emphasis on the effectiveness of surgery, complications, sexual and ...
Pradyumna Pan, Pan, Pradyumna
core   +1 more source

Advanced‐Stage Gonadal Dysgerminoma in a Patient With a Previous Diagnosis of Familial Swyer Syndrome: A Very Rare Genetic Entity

Case Reports in Medicine, Volume 2026, Issue 1, 2026.
Introduction Swyer syndrome is a genetic abnormality characterized by a 46,XY karyotype in a phenotypically female individual. Affected individuals typically have average or tall stature, unambiguous genitalia at birth, the presence of Müllerian structures, and bilateral streak gonads.
Süleyman Cemil Oğlak, Nilgün Söğütçü, Sedat Akgöl, Özgür Adıgüzel, Hümeyra Elif Ateş Eminoğlu, Gizem Güzel, Veysi Balcı, Emine Acar, Abdullah Acar, Fuat Bozan, Aneek Das Bhowmik   +10 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, Kacalska-Janssen, Olga, Płonka, Magdalena, Kłosowicz, Estera, Jach, Robert, Komenda, Justyna, Adrianowicz, Beata, Doroszewska, Katarzyna   +7 more
core   +1 more source

Conservative Management of Vaginal Hypoplasia

JCRPE, 2020
In patients with Mayer-Rokitansky-Küster-Hauser syndrome and complete androgen insensitivity syndrome (CAIS), management of vaginal hypoplasia includes non-surgical or surgical vaginal elongation techniques.
Özlem Dural, Şükran Poyrazoğlu
doaj   +1 more source