Results 81 to 90 of about 55,978 (163)

Magnetic resonance imaging in obstructive Müllerian anomalies

open access: yesJournal of Human Reproductive Sciences, 2013
Herlyn-Werner-Wunderlich (HWW) syndrome is a very rare congenital anomaly of the urogenital tract involving Müllerian ducts and Wolffian structures.
Kamal Kumar Sen   +2 more
doaj   +1 more source

Successful Vaginal Delivery of Naturally Conceived Dicavitary Twin in Didelphys Uterus: A Rare Reported Case

open access: yesCase 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

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

open access: yesJournal 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   +6 more
doaj   +1 more source

External validation of anti-Müllerian hormone based prediction of live birth in assisted conception [PDF]

open access: yes, 2013
<p>Background - Chronological age and oocyte yield are independent determinants of live birth in assisted conception. Anti-Müllerian hormone (AMH) is strongly associated with oocyte yield after controlled ovarian stimulation.
Grisendi, V.   +6 more
core   +1 more source

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

open access: yesUrology 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   +5 more
doaj   +1 more source

Persistent Mullerian duct syndrome with seminoma: report of a case

open access: yes, 1985
Persistent Mullerian duct syndrome is a male hermaphroditism in which remnants of Mullerian ducts occur from abnormality of Mullerian inhibitory factor and often cause transverse testicular ectopia or hernia uteri inguinalis.
若林, 昭   +5 more
core  

Batesian mimics influence mimicry ring evolution

open access: yes, 2003
Mathematical models of mimicry typically involve artificial prey species with fixed colorations or appearances; this enables a comparison of predation rates to demonstrate the level of protection a mimic might be afforded.
Noble, Jason   +5 more
core   +1 more source

Measurements of serum mullerian inhibiting substance in the evaluation of children with nonpalpable gonads [PDF]

open access: yes, 2014
At the time of publication, Mary Lee was not yet affiliated with the University of Massachusetts Medical School.BACKGROUND: Mullerian inhibiting substance, produced constitutively by the prepubertal testes, promotes involution of the mullerian ducts ...
Hasegawa, T.   +7 more
core   +1 more source

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

open access: yesAdvanced 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   +5 more
doaj   +1 more source

Septate uterus with cervical duplication and a longitudinal vaginal septum: an unclassified mullerian anomaly [PDF]

open access: yes, 2016
Uterine anomalies are the result of disturbances in the development, formation or fusion of the mullerian ducts during foetal life with an incidence of 0.001%-10% in general population.
Mangla, Ruchika   +2 more
core   +1 more source

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