Results 61 to 70 of about 368,247 (166)
ABSTRACT Here we present follow up of 3 cases of mid vaginal atresia and a functional uterus treated by single stage utero vaginal anastomosis using rectal tube insertion in uterus (for drainage) simultaneously with the amnion graft for vaginoplasty. This procedure successfully restored regular menstruation with fertility preservation and low morbidity.
Elham Askary +5 more
wiley +1 more source
Hysteroscopy metroplasty for partial septate uterus: Just a matter of infertility?
Abstract Objective The primary objective of this study is to assess the impact of hysteroscopic metroplasty on symptom relief, including dysmenorrhea, dyspareunia, and menstrual blood flow in women with partial uterine septa (U2a class). Additionally, the study aims to investigate potential correlations between clinical and ultrasonographic ...
Alessandro Arena +9 more
wiley +1 more source
Vaginal clear cell adenocarcinoma with associated Mullerian duct anomalies, renal agenesis and situs inversus: report of a case with no known in-utero exposure with diethyl stilboestrol [PDF]
A 27 year old female presented with two months history of continuous vaginal bleeding. On evaluation, she was diagnosed as a case of vaginal clear cell adenocarcinoma (VCCA) along with associated Mullerian duct anomalies including didelphys uterus with ...
Zeeshan-ud-din,, Ahsan, Aamir
core
DiI Analysis of Cell Migration during Mullerian Duct Regression
In most male vertebrates, the Mullerian ducts, which are the embryonic oviducts, regress completely during embryogenesis or shortly thereafter. Mullerian duct regression is caused by the testicular hormone Mullerian inhibiting substance.
Austin, Harriet B.
core +1 more source
Mayer–Rokitansky–Kuster–Hauser syndrome: Syndrome of Mullerian agenesis – A report of two cases
The Mayer–Rokitansky–Kuster–Hauser syndrome (MRKH syndrome), simply called Rokitansky syndrome or vaginal aplasia of the uterus, is a congenital condition that is characterized by the absence of the uterus and vagina, but ovaries are present and the ...
Sushma Yalavarthi +3 more
doaj +1 more source
A 6‐year‐old child with a rare dual diagnosis confirmed by genetic testing ‐ osteogenesis imperfecta (blue sclerae, disproportionate short stature) and concurrent 46,XY disorder of sex development (micropenis, hypospadias, impalpable gonads). ABSTRACT Osteogenesis imperfecta (OI) is a heritable disorder of type I collagen characterized by bone ...
Harshita Agarwal +4 more
wiley +1 more source
A case of recurrent cyst of Mullerian duct [PDF]
A case of recurrent cyst of Mullerian duct is reported. The patient had complained of dysuria and underwent resection of Mullerian duct cyst in May, 1977. Five years later (in July, 1982) at 50 years old, he again visited our clinic with the complaint of
平尾, 佳彦 +5 more
core
Transverse testicular ectopia with persistent mullerian duct syndrome
Transverse testicular ectopia is rarely associated with persistent mullerian duct syndrome, The ninth pediatric case of transverse testicular ectopia with persistent mullerian duct syndrome is reported, The clinical and operative findings and treatment ...
Tanyel, FERİDUN CAHİT +3 more
core +1 more source
Müllerian duct anomalies: review of current management
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 +1 more source
Mullerian anomalies: from diagnosis to intervention [PDF]
Background: The aim of the study was to observe prevalence of Mullerian anomalies, their clinical features, various investigation modalities to diagnose anomalies, various treatment modalities to correct anomalies and outcome after correction. Methods: A
Thakkar, Vidhi, Kapadia, Shital
core +1 more source

