Results 31 to 40 of about 7,671 (219)
Odontogenic keratocyst and uterus bicornis in nevoid basal cell carcinoma syndrome: Case report and literature review [PDF]
Nevoid basal cell carcinoma syndrome (NBCCS), an autosomal dominant disorder with a high degree of penetrance and variable expressivity, is characterized by basal cell carcinomas, odontogenic keratocysts, palmar and/or plantar pits and ectopic ...
F. MORGESE +3 more
core +1 more source
An atypical Müllerian duct anomaly: Duplicated cervices and vaginas with a single uterine cavity
Müllerian duct anomalies include a wide variety of developmental abnormalities involving the female reproductive system, many of which are not adequately represented by the current classification system used in the United States.
Ryan Narbutas, MD +4 more
doaj +1 more source
Septate uterus: nosographic overview and endoscopic treatment [PDF]
To comment on the prevalence, diagnosis, and treatment of the septate uterus, with special reference to hysteroscopic metroplasty and its effect on reproductive outcome, we searched publications in PubMed and Embase.
Cal\uec, G. +6 more
core +1 more source
Diagnosis and treatment of Müllerian anomalies: Experience at the Fundación HOMI
Background: Müllerian anomalies are rare developmental abnormalities. In the pediatric population, they manifest clinically during puberty and may require surgical treatment for symptom management.
Daniela Moreno Villamizar +7 more
doaj +1 more source
Laparoscopic Removal of Nonseparated Cavitated Horn in Unicornuate Uterus: Surgical Aspects and Long-Term follow-up [PDF]
Background: In unicornuate uterus cases, when the rudimentary horn is very close to the uterus and is firmly attached, laparoscopic surgery can be very challenging due to the danger of massive bleeding and the possiblity of damaging the healthy ...
Massimo Candiani +5 more
doaj +1 more source
Müllerian duct aplasia–renal agenesis–cervicothoracic somite dysplasia (MURCS) association is a rare and unusual constellation of nonrandom findings that include Müllerian duct aplasia, renal aplasia, and cervicothoracic somite dysplasia. The agenesis of
Reddy Ravikanth, Pooja Majumdar
doaj +1 more source
MRI Evaluation of Mullerian Duct Anomalies: Practical Classification by the New ASRM System
Mahasen S Al Najar,1 Nosaiba T Al Ryalat,1 Jaffer S Sadaqah,1 Rawand Y Husami,1 Karem H Alzoubi2,3 1Department of Diagnostic Radiology, The University of Jordan Hospital, Amman, Jordan; 2Department of Pharmacy Practice and Pharmacotherapeutics ...
Al Najar MS +4 more
doaj
MR assessment of Müllerian duct anomalies: Does it help?
Purpose: To evaluate the role of magnetic resonance imaging in diagnosis of Müllerian duct anomalies. Patients and methods: A prospective study included 48 female patients suspected to have Müllerian duct anomalies. All patients underwent trans-abdominal
Nadia F. El Ameen +2 more
doaj +1 more source
Background Müllerian duct anomalies are congenital malformations of the female genital tract and may be of various types. For decades they have been classified according to the American Society of Reproductive Medicine, which mentions unicornuate uterine
G. Gitas +6 more
doaj +1 more source
Müllerian Anomalies: Revisited
The Müllerian structures are developed from paired embryologic ducts that undergo fusion and resorption in utero to form the uterus, fallopian tubes, cervix, and upper two-thirds of the vagina.
Tulika Singh +3 more
doaj +1 more source

