Results 11 to 20 of about 2,520 (182)

Müllerian duct anomalies: review of current management [PDF]

open access: yesSão Paulo Medical Journal, 2009
The aim of this paper was to discuss the embryological aspects of Müllerian duct anomalies and to analyze the current diagnostic methods and therapy. Müllerian anomalies are congenital defects of the female reproductive tract resulting from failure in ...
Sérgio Conti Ribeiro   +6 more
doaj   +4 more sources

Persistent mullerian duct syndrome

open access: yesIndian Journal of Radiology and Imaging, 2010
AbstractPersistent Mullerian duct syndrome (PMDS) is a rare form of internal male pseudohermaphroditism in which Mullerian duct derivatives are seen in a male patient. This syndrome is characterized by the persistence of Mullerian duct derivatives (i.e.
Renu Divya, Rao B, Ranganath K, Namitha
openaire   +5 more sources

Genome-wide association study identifies common and low-frequency variants at the AMHgene locus that strongly predict serum AMH levels in males [PDF]

open access: yes, 2016
Anti-Müllerian hormone (AMH) is an essential messenger of sexual differentiation in the foetus and is an emerging biomarker of postnatal reproductive function in females.
Day, Felix R.   +5 more
core   +1 more source

Prevalence and diagnosis of congenital uterine anomalies in women with reproductive failure: a critical appraisal [PDF]

open access: yes, 2008
BACKGROUND: The prevalence of congenital uterine anomalies in women with reproductive failure remains unclear, largely due to methodological bias. The aim of this review is to assess the diagnostic accuracy of different methodologies and estimate the ...
Cocksedge, K.A.   +2 more
core   +1 more source

MULLERIAN DUCT ANOMALIES;

open access: yesThe Professional Medical Journal, 2012
Background: Müllerian duct anomalies (MDAs) occur with an incidence estimated to be 4.3%. A unicornuate uterus with orwithout a rudimentary horn; is a type of mullerian duct abnormality with a frequency of 0.4%. Rudimentary horn pregnancies are rare obstetriccomplication and may cause difficulty in diagnosis and subsequent management.
SARWAT ARA, TASNEEM ALI
openaire   +2 more sources

Cervical Dysgenesis: A Rare Mullerian Duct Anomaly [PDF]

open access: yesCureus, 2021
Cervical agenesis or dysgenesis is a rare congenital anomaly. The patients usually present with primary amenorrhoea, primary infertility, and cyclical abdominal pain or with a history of prior surgeries like hymenectomy, vaginoplasty, or adhesiolysis for endometriosis along with well developed secondary sexual characters.
Samantaray, Subha R, Mohapatra, Ipsita
openaire   +2 more sources

Müllerian inhibiting substance/anti-Müllerian hormone: A novel treatment for gynecologic tumors [PDF]

open access: yes, 2014
Müllerian inhibiting substance (MIS), also called anti-Müllerian hormone (AMH), is a member of the transforming growth factor-β super-family of growth and differentiation response modifiers.
Donahoe, Patricia K.   +2 more
core   +1 more source

Herlyn-Werner-Wunderlich syndrome : a rare genitourinary anomaly in females : a series of four cases [PDF]

open access: yes, 2018
We present case series of four patients with an important syndrome known as Herlyn-Werner-Wunderlich syndrome. Herlyn-Werner-Wunderlich syndrome is a rare congenital anomaly characterised by uterus didelphys with blind hemivagina and ipsilateral renal ...
Ilyas, Mohd   +2 more
core   +1 more source

Uterus Dysplasia Associated with Cervico-Vaginal Agenesis [PDF]

open access: yesInternational Journal of Fertility and Sterility, 2018
Müllerian ducts can form upper parts of normal female reproductive system and any failure in ductal fusion may result in to müllerian duct anomalies (MDA).
Ali Mahdavi   +4 more
doaj   +1 more source

The laboratory in the multidisciplinary diagnosis of differences or disorders of sex development (DSD)

open access: yesAdvances in Laboratory Medicine, 2021
46,XY differences/disorders of sex development (DSD) involve an abnormal gonadal and/or genital (external and/or internal) development caused by lack or incomplete intrauterine virilization, with or without the presence of Müllerian ducts remnants.
Granada Maria Luisa, Audí Laura
doaj   +1 more source

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