نتایج جستجو برای: mullerian anomaly
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Accessory fallopian tube is a rare, congenital and developmental mullerian duct anomaly. The documented incidence around 6-10% in women seeking for infertility treatment. We observed accessory patient during routine checking of operative field, ovaries caesarean section. anomaly which attached with ampullary part main tube. common site pyosalpinx, hydrosalpinx, cystic swelling torsion can lead ...
Rudimentary horn is an anatomic variant of unicornuate uterus which a mullerian duct anomaly resulting from the incomplete fusion ducts. The prevalence congenital uterine malformations about 3.2%Pregnancy in rudimentary extremely rare condition occurring 1 76,000 to 1,40,000 pregnancies. Unicornuate with maybe associated gynecological and obstetric complications like infertility, endometriosis,...
Objective: The aim of the present study is to evaluate etiologic factors in patients with recurrent pregnancy loss (RPL). Material and methods: The records of patients admitted to Obstetrics& Gynecology Clinic of Dicle University Medical Faculty Hospital, from 2008 to 2011 were evaluated. Of the 114 patients who all tests were applied for diagnosis in our hospital were enrolled to study. For et...
Biconuate uterin is a congenital anomaly of the mullerian duct that can be associated with many complications. A 34-year-old woman was admitted because of having labor pain. She was using an IUD contraceptive device that was not successful in her case. Because of Breech malpresentation and a previous cesarean section, she was scheduled for cesarean section. During the surgery, the presence of t...
Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is a congenital anomaly of female genital tract where there hypoplasia uterus and upper two- thirds vagina. Patients with MRHK present normal development secondary sexual characteristics due to ovarian function. We report 2 cases who presented absent ovaries confirmed on imaging. Both our MRKH had short stature underdeveloped characteristics. It ex...
Herlyn-Werner-Wunderlich (HWW) syndrome is a very rare congenital anomaly of the urogenital tract resulting from maldevelopment of both Mullerian and Wolffian ducts. It is characterized by the triad of uterus didelphys, obstructed hemivagina and ipsilateral renal agenesis. It generally presents at puberty shortly following menarche with the symptom of acute pelvic pain. Management of these case...
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