Results 31 to 40 of about 657,319 (150)

Case report: Persistent Müllerian duct syndrome and enlarged prostatic utricle in a male dog

open access: yesFrontiers in Veterinary Science, 2023
A 1-year-old male intact Miniature Schnauzer mix was presented for chronic intermittent hematuria. Abdominal ultrasonography revealed a large, fluid-filled cystic structure extending cranially and dorsally to the prostate. Computed tomography scan images
Peter J. Welsh   +8 more
doaj   +1 more source

Anterior bladder flap neo urethra as treatment for stress urinary incontinence due to developmental urogenital anomaly

open access: yesUrology Annals, 2013
Congenital anomalies that involve the distal segment of urogenital sinus (giving rise to female urethra and vagina) may lead to abnormal urethral development ranging from absent to markedly deficient urethra.
N Rajamaheswari   +3 more
doaj   +1 more source

Operative cystoscopy in the neonatal period

open access: yesLa Pediatria Medica e Chirurgica, 2016
Aim of the study is to report the experience in the last three years about endourological treatment of newborns affected by genito- and urinary malformation, implying critical urinary tract dilatation and bladder mass requiring a neonatal operative ...
Salvatore Arena   +3 more
doaj   +1 more source

Persistent Urogenital Sinus (PUGS) Anomaly in Children: A Single Center Experience [PDF]

open access: yesJournal of Chemical Health Risks
Background: Urogenital sinus (UGS) or Persistent urogenital sinus (PUGS) is an uncommon congenital malformation characterized by failure of normal separation of the urinary and genital tract during embryonic development.It may present as an isolated ...
MD. Nazrul Islam
openaire   +2 more sources

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

Surgical Treatment After Failed Primary Correction of Urogenital Sinus in Female Patients with Virilizing Congenital Adrenal Hyperplasia.

open access: yesFrontiers in Pediatrics, 2016
Purpose: Genital reconstruction in female patients with virilizing congenital adrenal hyperplasia (CAH) is very challenging. Our aim was to evaluate the techniques employed to treat complications after failure of primary urogenital sinus (UGS) surgery ...
Maria Helena Palma Sircili   +6 more
doaj   +1 more source

Laser neoureterocystostomy to treat ectopic ureters

open access: yesEquine Veterinary Journal, EarlyView.
Abstract Background Ureteral ectopia is an uncommon but clinically important congenital abnormality in horses. If left untreated, it can lead to persistent dermatitis, urinary tract infections, and failure to thrive. Surgical correction is necessary, but traditional approaches have produced mixed results with high morbidity.
Caitlin Smith, Eric J. Parente
wiley   +1 more source

Persistent hyper-programs [PDF]

open access: yes, 2011
This work was supported by ESPRIT III Basic Research Action 6309 – FIDE 2 and SERC grant GR/F 02953.The traditional representation of a program as a linear sequence of text forces a particular style of program construction to ensure good programming ...
Dearle, Alan   +5 more
core   +2 more sources

Pelvic Exenteration for Cervical Cancer: Oncological, Morbidity and Quality of Life Outcomes

open access: yesJournal of Surgical Oncology, EarlyView.
ABSTRACT Background and Objectives One third of patients who undergo definitive chemoradiotherapy for locally advanced cervical cancer develop disease recurrence. Salvage surgery in the form of pelvic exenteration (PE) may offer improved survival and possibly cure in carefully selected patients, however robust data is scarce.
Alexandra M. Peacock   +6 more
wiley   +1 more source

The Audiologic and Otolaryngologic Phenotype in WHIM Syndrome

open access: yesOtolaryngology–Head and Neck Surgery, EarlyView.
Abstract Objective WHIM syndrome (warts, hypogammaglobulinemia, infections, and myelokathexis syndrome) is an ultra‐rare primary immunodeficiency disease caused by autosomal dominant hyperfunctional mutations in the chemokine receptor CXCR4. Otolaryngologists are frequently consulted to evaluate WHIM patients because of recurrent acute ear and sinus ...
Christopher K. Zalewski   +7 more
wiley   +1 more source

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