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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   +6 more sources

Mayer-Rokitansky-Kuster-Hauser syndrome [PDF]

Revista Brasileira de Ginecologia e Obstetrícia
•Mayer-Rokitansky-Kuster-Hauser syndrome (MRKH) is the leading cause of vaginal agenesis. •It is characterized by primary amenorrhea with typical adrenarche and telarche and may be associated with congenital urological and skeletal conditions that should be investigated.
Claudia Cristina Takano Novoa, Mila Torii Correa Leite, Marair Gracio Ferreira Sartori   +2 more
doaj   +4 more sources

Mayer Rokitansky Kuster Hauser Syndrome

Andalas Obstetrics and Gynecology Journal, 2023
Mayer Rokitansky Küster Hauser syndrome (MRKH) is a syndrome characterized by uterine, cervix, and the two third of upper vagina aplasia which is the cause of incomplete development of the Müllerian duct.
Arga Kafi Perdana Kusuma, Bobby Indra Utama   +1 more
doaj   +2 more sources

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

Incidental Finding of Leiomyoma in Mayer-Rokitansky-Kuster-Hauser Syndrome [PDF]

Journal of Investigative Medicine High Impact Case Reports, 2021
Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is a sexual developmental disorder. In this disorder, there is a congenital absence of the uterus and vagina with normal external genitalia. The etiology is not well understood. Variations of this condition exist that may include congenital abnormalities and psychological problems.
Jerome Okudo
exaly   +4 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 Agenesis in Mayer Rokitansky Kuster Hauser Syndrome [PDF]

Medical Journal Armed Forces India, 2009
The Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is characterized by congenital aplasia of the uterus and the upper part (2/3) of the vagina. The first sign of MRKH syndrome is primary amenorrhea in young women presenting otherwise with normal development of secondary sexual characteristics and normal external genitalia, with normal and functional ...
A, Menon, M, Biswas, Sps, Kochar, H, Bal, R, Abhichandani, S, Singh   +5 more
exaly   +3 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

Mayer-Rokitansky-Kuster-Hauser syndrome: a review

International Journal of Women's Health, 2015
Laura Londra, Farah S Chuong, Lisa KolpDivision of Reproductive Endocrinology and Infertility, Department of Gynecology and Obstetrics, Johns Hopkins University, Baltimore, MD, USAAbstract: The congenital aplasia or severe hypoplasia of mullerian ...
Londra L, Chuong FS, Kolp L
doaj   +5 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