Results 101 to 110 of about 449,820 (222)

A Case of Mayer–Rokitansky–Küster–Hauser Syndrome with a Fused Pancake-shaped Pelvic Kidney

Advanced Biomedical Research, 2019
Mayer–Rokitansky–Küster–Hauser (MRKH) Syndrome is a female reproductive system disorder. It is characterized by a defect in the Müllerian ducts development, and it causes the absence of the uterus in variable degrees in upper vaginal hypoplasia.
Ali Reza Eftekhari Moghadam, Ghasem Saki, Mahin Taheri Moghadam, Seyed Mohamad Hossein Mohseni, Vajieh Heidari, Mohammad Hossein Jamshidi   +5 more
doaj   +1 more source

Complete transverse vaginal septum complicated by pyocolpos, primary vesicoureteral reflux and ectopic ureter with renal loss: a case report

Urology Case Reports
A transverse vaginal septum is a rare Müllerian anomaly caused by incomplete fusion between the Müllerian ducts and the urogenital sinus. It can obstruct menstrual flow, leading to hematocolpos, hydrocolpos, or pyocolpos.
Izadora Gabriela Coutinho, Paulo Acácio Egger, Ailton Fernandes Junior, Angelo Cezar Bolognese Junior, Abikeilla Ariane Bomfim Gomes Bernardi, Amanda Yumi Ono Valderrama   +5 more
doaj   +1 more source

Partial Cervico-Vaginal Aplasia with Functional Endometrium: A Case Report On a Simple Recanalization Technique for Outflow Reconstruction in Low-Resource Settings

Journal of Gandhara Medical and Dental Sciences
A 13- year- old girl presented with cyclical pelvic pain and primary amenorrhea, revealing a rare complex cervicovaginal hypoplasia with hematometra. Diagnosis was confirmed through clinical examination, ultrasound, and MRI, emphasizing the importance ...
Naheed Parveen, Sadia Shoukat, Erum Samreen Siddiqui, Sakeena Ahmed4, Nadia Shoukat   +4 more
doaj   +1 more source

Blood in semen as a clue

Revista de la Facultad de Ciencias Médicas de Córdoba
A 21-year-old man presented with blood in his semen and was diagnosed with Persistent Müllerian Duct Syndrome (PMDS). This rare genetic condition occurs due to insufficient Anti-Müllerian Hormone (AMH) production or AMH insensitivity, resulting in the ...
Jheniffer Cação, Thais de Paiva Guimarães Barreiro, Thaís Nogueira Dantas Gastaldi, Márcio Luís Duarte   +3 more
doaj   +1 more source

Clinical aspects of Mayer-Rokitansky-Kuester-Hauser syndrome: recommendations for clinical diagnosis and staging [PDF]

, 2017
BACKGROUND: The Mayer-Rokitansky-Kuester-Hauser (MRKH) syndrome is a malformation of the female genitals (occurring in one in 4000 female live births) as a result of interrupted embryonic development of the Müllerian (paramesonephric) ducts.
Beckmann, Matthias W., Brucker, Sara, Hauser, Georges A., Kellermann, Anja, Ludwig, Kurt S., Oppelt, Peter, Renner, Stefan P., Strick, Reiner, Strissel, Pamela L., Wallwiener, Diethelm   +9 more
core  

Ovarian dysgerminomas are characterised by frequent KIT mutations and abundant expression of pluripotency markers [PDF]

, 2007
Background Ovarian germ cell tumours (OGCTs) typically arise in young females and their pathogenesis remains poorly understood. We investigated the origin of malignant OGCTs and underlying molecular events in the development of the ...
Hoei-Hansen, Christina E, Kraggerud, Sigrid M, Abeler, Vera M, Kærn, Janne, Rajpert-De Meyts, Ewa, Lothe, Ragnhild A   +5 more
core   +1 more source

Uterine Rupture: Fifteen Weeks of Non-communicating Uterine Horn Pregnancy

Bagcilar Medical Bulletin
We evaluated the management of a ruptured non-communicated rudimentary horn pregnancy at the 15th gestational week. A 22-year-old multigravida who was detected to have a 15-week pregnancy according to her last menstrual period was admitted to our clinic ...
Ömer Faruk Bayraktar, Sevde Nur Su, Tolga Karacan, Hakan Güraslan   +3 more
doaj   +1 more source

Müllerian Agenesis Masquerading as Secondary Amenorrhea

Case Reports in Pediatrics, 2018
The most common cause of primary amenorrhea is congenital malformation of the Müllerian ducts, including Müllerian agenesis, also known as Mayer–Rokitansky–Küster–Hauser syndrome (MRKH).
Gloria Tavera, Rina Lazebnik
doaj   +1 more source

Unicornuate Uterus with Non-communicating Rudimentary Horn: A Case Report [PDF]

Journal of Clinical and Diagnostic Research
Müllerian malformations are structural anomalies of the female genital tract due to failure of fusion or development of the paramesonephric (Müllerian) ducts.
Udhayalakshmi Thirumal, P Pallavee, Divya Alamelu, Thota Anusha Reddy, E Nandhini   +4 more
doaj   +1 more source

Herlyn-Werner-Wunderlich Syndrome with Degenerating Fibroid– Uncommon Presentation of a Rare Anomaly [PDF]

Journal of Krishna Institute of Medical Sciences University, 2018
Herlyn-Werner-Wunderlich Syndrome (HWWS) is a rare congenital anomaly of Mullerian and mesonephric ducts characterized by uterus didelphys with obstructed hemivagina and ipsilateral renal agenesis.
Kanakaraj Kannan, N Pavan Kumar, Venkatraman Indiran, T Ramachandra Prasad, Prabakaran Maduraimuthu   +4 more
doaj