Results 1 to 10 of about 1,485 (129)

Retrograde menses presented as acute stump appendicitis- Mayer-Rokitansky-Küster-Hauser syndrome [PDF]

Radiology Case Reports
Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is an exceptionally rare condition. This article highlights its unusual presentation and the role of radiological imaging in the diagnosis and outlines an approach to management.
Mohammad Mohsin Arshad, MBBS, MD, Devendra Kumar, MBBS, Nouran Eltantawi, MBBS, Muhammad Junaid Iqbal, MBBS   +3 more
doaj   +2 more sources

Long-Term Psychosocial Outcomes in Japanese Mayer-Rokitansky-Küster-Hauser Syndrome: A Single-Center Study. [PDF]

J Obstet Gynaecol Res
ABSTRACT Aim Vaginal creation enables sexual intercourse in patients with Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome. However, long‐term psychosocial outcomes, particularly in Japanese patients, remain underreported. This study aimed to explore the long‐term psychosocial outcomes associated with different choices of vaginal creation in patients ...
Okunomiya A, Tsuyuki K, Ohsuga T, Ohara T, Yanai A, Mizuno R, Yamanoi K, Egawa M, Mandai M.   +8 more
europepmc   +2 more sources

Recurrent ovarian inguinal hernia complicated with Mayer–Rokitansky–Küster–Hauser syndrome: a case report [PDF]

Journal of Medical Case Reports
Background Herniation of female genital organs complicated by Mayer–Rokitansky–Küster–Hauser syndrome in adolescents is rarely reported in previous studies, and delayed diagnosis or misdiagnosis of this situation can lead to serious injury.
Weichao Liang, Qisheng Chen, Yihao Ma, Yingchang Zhu   +3 more
doaj   +2 more sources

Vaginal endometriosis following uterine transplantation in a patient with Mayer-Rokitansky-Küster-Hauser syndrome: A unique case report. [PDF]

Int J Gynaecol Obstet
International Journal of Gynecology &Obstetrics, Volume 172, Issue 3, Page 1794-1795, March 2026.
Moravcova J, Chmel R, Maluskova J, Sticova E.   +3 more
europepmc   +2 more sources

Mayer-Rokitansky-Küster-Hauser syndrome type II: A rare case report [PDF]

SAGE Open Medical Case Reports
MRKH syndrome, or Mayer-Rokitansky-Küster-Hauser syndrome, a rare congenital disease, manifests as a complete or partial aplasia of the uterus and the vagina’s upper two-thirds with normal external genitalia and functioning ovaries.
Kaouthar Sfar, Kaoutar Imrani, Fatima Chait, Sara Essetti, Kaoutar Maslouhi, Nabil Moatassim Billah, Ittimade Nassar   +6 more
doaj   +2 more sources

Rectovaginal fistula in a patient with Mayer-Rokitansky-Kuster-Hauser syndrome [PDF]

Urology Case Reports
MRKH syndrome is defined by the congenital absence of the uterus and the upper two-thirds of the vagina in females, who otherwise exhibit normal secondary sexual characteristics and possess a typical 46, XX karyotype. Here we report a case of 23 year old
Puvvada Sandeep, S. Shanthakumar, Venkata Mahesh Chalumuru, D. Ramesh, Tarun Dilip Javali   +4 more
doaj   +2 more sources

Rare Association of Mayer–Rokitansky–Kuster–Hauser Syndrome with Rectovestibular Fistula and Colonic Atresia [PDF]

Journal of Indian Association of Pediatric Surgeons
Rectovestibular fistula is the most common presentation of female anorectal malformation. Its association with Mayer–Rokitansky–Kuster–Hauser (MRKH) syndrome and Colonic atresia is uncommon.
Audrey Pais, Parag Karkera, Pradnya S. Bendre, Siddhi Sanglikar, Hemant Pikale, Minnie Bodhanwala   +5 more
doaj   +2 more sources

A Novel Association of Colonic Duplication with Mayer–Rokitansky–Kuster–Hauser Syndrome in an Adolescent Girl [PDF]

Journal of Indian Association of Pediatric Surgeons
The association is defined as two or more malformations with unclear relationships, which do not fit the criteria of a syndrome. This case report presents a rare finding of tubular colonic duplication in association with Mayer–Rokitansky–Küster–Hauser ...
Rajib Bora, Sheetal Upreti, Gaurav Saxena, Sujoy Neogi, Simmi K. Ratan   +4 more
doaj   +2 more sources

Mayer-Rokitansky-Kuster-Hauser syndrome [PDF]

Revista Brasileira de Ginecologia e Obstetrícia
Claudia Cristina Takano Novoa, Mila Torii Correa Leite, Marair Gracio Ferreira Sartori   +2 more
doaj   +2 more sources

Hollow vaginal stent for a case of Mayer-Rokitansky-Kuster-Hauser syndrome: a case report

The Pan African Medical Journal, 2021
Congenital vaginal agenesis is a common condition with an instance of 1 in 5000 females. It is usually associated with Mayer-Rokitansky-Kuster Hauser syndrome. Such anomalies have a high impact on the physiology and psychology of patients.
Sharayu Vinod Nimonkar, Vikram Murlidhar Belkhode   +1 more
doaj   +1 more source