Results 51 to 60 of about 125,080 (190)

Absorption of the Wolffian duct and duplicated ureter by the urogenital sinus: morphological study using human fetuses and embryos

open access: yes, 2015
Objectives To describe the embryological origin of the duplicated ureter and to investigate whether the urogenital sinus absorbs not only the Wolffian duct (WD) but also the ureter.
Jose Francisco Rodriguez‐Vazquez   +11 more
core   +1 more source

Hydrometrocolpos Due to Persistent Urogenital Sinus Mimicking Neonatal Ascites [PDF]

open access: yes, 2008
Objective: A urogenital sinus is a common channel into which both the urethra and genital tracts open. Occasionally there might be transverse obstructing membrane leading to hydrometrocolpos from either uterine secretions or urine.
Ghani, Imran   +2 more
core   +1 more source

Transsphinctericanorectal reconstruction of ambiguous genitalia: an innovative approach to neovaginoplasty, pioneer in Brazil

open access: yesSão Paulo Medical Journal
The authors, based upon previous experience in the treatment of ten children with cloacal abnormalities, among which two with female pseudohermaphroditism with cloaca, hereby present a pioneer experience in Brazil, with the "posterior sagittal ...
Albany Braz   +1 more
doaj   +1 more source

Posterior cloaca: Multicenter experience of a very rare and unusual anorectal and genitourinary malformation

open access: yesJournal of Indian Association of Pediatric Surgeons, 2022
Aim: Posterior cloacal malformations (PCMs) are distinguished from classical cloacal malformations by the posterior location of the common opening in the perineum.
Rohit Kapoor   +3 more
doaj   +1 more source

Simultaneous Ureterovaginal and Rectovaginal Fistulas Caused by a Cube Pessary: A Case Report

open access: yesIJU Case Reports, Volume 9, Issue 6, November 2026.
ABSTRACT Introduction We present a case of simultaneous ureterovaginal and rectovaginal fistulas caused by continuous placement of a cube pessary without daily removal, successfully managed through a multidisciplinary approach. Case Presentation An 84‐year‐old female managed with a cube pessary presented with hematochezia.
Tetsuhiro Yano   +9 more
wiley   +1 more source

Primary BPH Stromal Cell Cultures Exhibit Heightened Androgen‐Responsiveness

open access: yesThe Prostate, Volume 86, Issue 15, Page 1508-1517, November 2026.
ABSTRACT Background Benign prostatic hyperplasia (BPH) is the most common disease in aging males. BPH growth is androgen‐dependent, and it appears that androgens preferentially stimulate the growth of BPH as compared to normal prostate. The mechanism of preferential androgen stimulation of BPH growth is not clear.
Wei Chen   +9 more
wiley   +1 more source

Renal Trichodinosis in the Japanese Rice Fish, Oryzias latipes: First Report and Phylogenetic Classification

open access: yesJournal of Fish Diseases, Volume 49, Issue 11, November 2026.
ABSTRACT Investigation of a disease outbreak in a hobbyist's medaka (Oryzias latipes) collection led to the detection of Trichodina sp. in the kidney tubuli of individual fish. Based on this observation, a thorough clinical workup, including native microscopy, histopathology and molecular genetics, was conducted.
J. Harl   +3 more
wiley   +1 more source

Congenital clitoromegaly in an adult

open access: yesThe Pan African Medical Journal, 2019
Clitoromegaly is an abnormal enlargement of the clitoris. In adult, dimensional criteria are, according to Brodie, a minimum length hood and width of 27.4mm and 8mm.
Mohammed Alae Touzani, Imad Ziouziou
doaj   +1 more source

An integrated imaging approach for diagnosis of cervico-vaginal outflow defects and associated genital anomalies

open access: yesThe Egyptian Journal of Radiology and Nuclear Medicine, 2015
Objective: The objective of this study was to evaluate the diagnosis of cervico-vaginal outflow anomalies using different ultrasound approaches (transabdominal, endoluminal and transperineal) and magnetic resonance imaging.
Soha Talaat Hamed   +2 more
doaj   +1 more source

The Homozygous p.(Arg215Ter) Variant in XRCC2 Is Associated With Atypical Fanconi Anemia Without Major Hematological Abnormalities in Childhood

open access: yesAmerican Journal of Medical Genetics Part A, Volume 200, Issue 10, Page 2331-2337, October 2026.
ABSTRACT Fanconi Anemia (FA) is the most frequent inherited bone marrow failure syndrome. A role for the XRCC2 gene in FA was suspected in 2012 and confirmed in 2016, but only two affected individuals have been described thus far, and no long‐term follow‐up is available.
Sabina Cenciarelli   +11 more
wiley   +1 more source

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