Results 31 to 40 of about 2,384 (209)
A Rare Obstetric Outcome in Uterus Didelphys with Obstructed Hemivagina and Ipsilateral Renal Agenesis [PDF]
, 2012 Background: The unique clinical syndrome of uterus didelphys, obstructed hemivagina, and ipsilateral renal anomaly is very rare and can be quite difficult to recognize because of the enormous heterogeneity in its clinical presentation.
Francisco, C +3 more
core +1 more source
An unusual diagnosis of a bicornuate unicollis uterus [PDF]
, 2008 We present a case of an unusual diagnosis of a bicornuate unicollis uterus mimicking a uterus didelphys with blind hemivagina. Few cases of a bicornuate uterus have been reported with the primary symptom of a paracervical pyocolpos.
Foidart, Jean-Michel +2 more
core +1 more source
Uterine didelphys with concomitant renal anomalies in both mother and fetus
Journal of Pediatric Surgery Case Reports, 2016 Uterine didelphys results from impaired fusion of the paired Müllerian ducts. The incidence of uterine anomalies is believed to be 0.5–2.0% of reproductive-age women, with didelphic uterus accounting for approximately 10%. Uterine didelphys is associated
Maren Boehnke +5 more
doaj +1 more source
Anorectal agenesis with rectovaginal fistula associated with uterus didelphys and vaginal septum
Journal of Pediatric Surgery Case Reports, 2020 Anorectal agenesis with rectovaginal fistula are extremely rare type of anorectal malformations (ARM) characterized by the absence of the anus and abnormal connection of the rectum to the vagina.
Maher AlZaiem +3 more
doaj +1 more source
Uterus Didelphys dengan Agenesis Servik Bilateral
Andalas Obstetrics and Gynecology Journal, 2020 LATAR BELAKANG : Anomali duktus mullerian adalah kelainan kongenital sistem reproduksi wanita yang disebabkan oleh perkembangan embriologis yang abnormal selama dalam kandungan.
Dwinda Rizary, Dedy Hendry
doaj +1 more source
22q11 Deletion Syndrome and Urogenital Manifestations: A Clinicopathological Case Report. [PDF]
, 2016 Deletion in the chromosomal region 22q11 results from the abnormal development of the third and fourth pharyngeal pouches during embryonic life and presents an expansive phenotype with more than 180 clinical features described that involve every organ ...
Ben Ali, N. +6 more
core +1 more source
Uterine Didelphys in a G4P3+0: A Disturbing Phenomenon at Caesarean Section [PDF]
Women’s Health Bulletin, 2023 Introduction: Uterine didelphys is an exceptionally rare Müllerian duct anomaly that, when incidentally discovered, can be profoundly disconcerting for attending clinicians, patients, and their families.
Abdibasid Ali +3 more
doaj +1 more source
Case Reports in Obstetrics and Gynecology, 2017 Didelphys uterus, or double uterus, is an embryological developmental malformation of the müllerian ducts with the incidence of approximately 8.3% of all müllerian duct abnormalities (MDAs).
Houda Nasser Al Yaqoubi, Nishat Fatema
doaj +1 more source
Pregnancy in uterus didelphys delivered by caesarean section: a case report [PDF]
, 2017 The aim of this study is to report a rare case of pregnancy in uterus didelphys. Mullerian duct anomalies are congenital defects of the female genital system that arise from abnormal embryological development of the Mullerian ducts.
Sawai, Devashish Singh +5 more
core +2 more sources
Uterine Carcinosarcoma in a Patient with Didelphys Uterus
Case Reports in Obstetrics and Gynecology, 2013 Background. Didelphys uterus is a noncommon finding in women. Till now, few cases with benign mesenchymal tumors in patients with didelphys uterus are described. We present a case of a patient with carcinosarcoma arising in a didelphys uterus. Case. A 73-
C. Iavazzo +4 more
doaj +1 more source