Results 71 to 80 of about 57,246 (159)

Müllerian duct cyst misdiagnosed as ovarian cyst: a rare case report [PDF]

, 2016
The Müllerian duct cyst is a remnant of the caudal ends of the fused embryologic paramesonephric ducts (or Müllerian ducts). Preoperative distinction of ovarian cyst from a Müllerian duct cyst is important and is based on visualization of the ipsilateral
Mishra, Vandana, Radhakrishnan, Gita, Shree, Sneha, Singh, Alpana   +3 more
core   +1 more source

Asynchronous twin delivery in uterus didelphys with a 12-week interval: case report and literature review

BMC Pregnancy and Childbirth
Background Uterus didelphys, or“double uterus,”is caused by the failure of Müllerian ducts fusion, eventually forming two uterine cavities, and it is one of the rare uterine malformations.Uterus didelphys and twin pregnancies are extremely rare ...
Huijie Liu, Chunxiao Zhou, Yingxin LV, Gaoxia Dong, Hui Qi   +4 more
doaj   +1 more source

OSR1 disruption contributes to uterine factor infertility via impaired Müllerian duct development and endometrial receptivity

The Journal of Clinical Investigation, 2023
Three sisters, born from consanguineous parents, manifested a unique Müllerian anomaly characterized by uterine hypoplasia with thin estrogen-unresponsive endometrium and primary amenorrhea, but with spontaneous tubal pregnancies.
Adriana Lofrano-Porto, Sidney Alcântara Pereira, Andrew Dauber, Jordana C.B. Bloom, Audrey N. Fontes, Naomi Asimow, Olívia Laquis de Moraes, Petra Ariadne T. Araujo, Ana Paula Abreu, Michael H. Guo, Silviene F. De Oliveira, Han Liu, Charles Lee, Wendy Kuohung, Michella S. Coelho, Rona S. Carroll, Rulang Jiang, Ursula B. Kaiser   +17 more
doaj   +1 more source

Minimally invasive management of Müllerian anomalies in pediatric patients: A retrospective case series and literature review

Journal of Pediatric Surgery Open
Müllerian anomalies (MA) are structural defects that arise due to alterations in the development of the paramesonephric or Müllerian ducts during the first 16 weeks of gestation. Few cases have been reported on laparoscopic management as a diagnostic and
Mario Riquelme, Juan Pelayo, Irving Cardenas-Medina, Ana Cantu-Zendejas, Alejandro Cendejas-Higuera, Eduardo Olazabal, Mario Palafox   +6 more
doaj   +1 more source

Mullerian ducts anomaly of 2 divergent uterine horns with cervicovaginal hypoplasia: Is it considered unclassified or under the spectrum of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome? [PDF]

Radiol Case Rep, 2023
Jaha G, AlMutairi B.
europepmc   +1 more source

37,X/38,XY Mosaicism in a Cryptorchid Bengal Cat with Müllerian Duct Remnants [PDF]

, 2015
A 23-month-old tomcat was referred to our clinic because of male behavioral problems, cryptorchidism, and an undefined intra-abdominal organ resembling a uterus.
Reichler, Iris, Grest, Paula, Balogh, Orsolya, Pieńkowska-Schelling, Aldona, Janett, Fredi, Reichler, Iris M, Janett, Fredy, Schelling, Claude, Berger, Alice, Willmitzer, Florian, Pienkowska-Schelling, A   +10 more
core   +2 more sources

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

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

DMRT1 is required for Müllerian duct formation in the chicken embryo [PDF]

, 2015
DMRT1 is a conserved transcription factor with a central role in gonadal sex differentiation. In all vertebrates studied, DMRT1 plays an essential function in testis development and/or maintenance.
Ayers, K.L., Roeszler, K.N., Cutting, A.D., Smith, C.A., Sinclair, A.H.   +4 more
core   +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