Obstructed Hemivagina and Ipsilateral Renal Agenesis Syndrome: A Case Report
Journal of Nepal Medical Association, 2022 Obstructed hemivagina and ipsilateral renal anomaly syndrome also known as Herlyn-Werner-Wunderlich syndrome is a rare congenital urogenital anomaly characterised by Mullerian duct anomalies associated with mesonephric duct anomalies.
Ashok Chapagain +3 more
doaj +1 more source
Classification conundrum: Persistent mullerian duct syndrome with hypospadias
Archives of Medicine and Health Sciences, 2016 The disorders of sex development (DSD) are uncommon and have wide phenotypic variation. Due to this, they often cannot be classified properly and go unreported.
Sheetal Arora, Ashish Kumar Mandal
doaj +1 more source
Obstructed hemivagina and ipsilateral renal anomaly (OHVIRA) syndrome: A case report
Journal of Pediatric Surgery Case Reports, 2023 Background: Obstructed hemivagina and ipsilateral renal anomaly (OHVIRA) or Herlyn-Werner-Wunderlich syndrome, is a rare Mullerian duct anomaly with uterus didelphys, unilateral obstructed hemivagina, and ipsilateral renal agenesis.
Mohamed Amin Elgohary +4 more
doaj +1 more source
An eventful journey from menarche to successful motherhood
Journal of Human Reproductive Sciences, 2016 Herlyn–Werner–Wunderlich syndrome is an uncommon variant of mullerian duct anomaly and the approach to its diagnosis requires a high index of suspicion and vigilant work up. Presented here is a case of a 26yearold woman who had the aforementioned anomaly
Salil B Chakrabarti +3 more
doaj +1 more source
Symptomatic Müllerian Duct Cyst in a Male Adult: A Rare Case Report [PDF]
, 2017 Background: Müllerian duct cyst is an uncommon congenital anomaly. It is usually small and asymptomatic. A rare case of this entity with symptoms of ejaculatory duct obstruction such as hematospermia and secondary infertility is presented here.Case ...
Shabaninia, Shahram +1 more
core +1 more source
Müllerian duct anomalies: review of current management [PDF]
, 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 ...
Edmund Chada Baracat +6 more
core +2 more sources
Azoospermia in a Male with Klippel–Feil Anomaly
Urology Case Reports, 2017 Müllerian-duct aplasia, renal agenesis, and cervical somite dysplasia (MURCS) is a rare genetic disorder. Previously thought to be exclusive in females, there have now been a small number of case reports describing a male analogue.
Maria Uloko +2 more
doaj +1 more source
Magnetic Resonance Imaging (MRI) Depiction of Robert's Uterus: A Rare Müllerian Duct Anomaly Presenting with Cyclical Pain in Young Menstruating Woman. [PDF]
Pol J Radiol, 2017 BACKGROUND: Robert's uterus is a very rare müllerian duct anomaly which is characterised by septate uterus with obstruction of a one-sided cavity and formation of hematometra.
Mittal P +5 more
europepmc +2 more sources
The Anatomical Record, EarlyView.Abstract Sexual differentiation in the equine fetus involves coordinated morphogenetic processes that shape both the gonads and the genital ducts. Although the formation of testes and ovaries has been relatively well documented, the temporal dynamics and morphometric patterns of the mesonephric (Wolffian) and paramesonephric (Müllerian) ducts remain ...
Tais Harumi de Castro Sasahara +4 more
wiley +1 more source
A transgenic bacterial artificial chromosome approach to identify regulatory regions that direct Amhr2 and Osterix expression in Müllerian duct mesenchyme [PDF]
, 2022 International audienceA transgenic mouse approach using bacterial artificial chromosomes (BAC) was used to identify regulatory regions that direct Müllerian duct expression for Amhr2 and Osterix (Osx, also known as Sp7).
Behringer, Richard, R +11 more
core +1 more source