Zobrazeno 1 - 10
of 165
pro vyhledávání: '"Andrea Bischoff"'
Autor:
Veronica I. Alaniz, Kelly Harris, Kellie Woodfield, Julie Friedman, Vatche Melkonian, Andrea Bischoff
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 110, Iss , Pp 102873- (2024)
Introduction: During cloacal reconstruction, vaginal replacement with an intestinal graft is considered when native vagina does not reach the perineum. Risks include need for revision surgery, mucus production, colitis, and rarely dysplasia. Given th
Externí odkaz:
https://doaj.org/article/08f2c9cd6902484a97dcd764c2b9ee54
Autor:
Vatche Melkonian, Luis de la Torre, Jill Ketzer, Victor Rodriguez, Alberto Pena, Andrea Bischoff
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 102, Iss , Pp 102777- (2024)
Introductions: Three patients presented with a colo-cutaneous fistula from the neo-rectum to previous laparoscopic port sites, following an otherwise technically correct pull-through for Hirschsprung disease. We evaluated each case to provide guidanc
Externí odkaz:
https://doaj.org/article/7d7e806d82e34ce4b140b43661923dc9
Publikováno v:
Urology Case Reports, Vol 51, Iss , Pp 102602- (2023)
Cloacal exstrophy, also known as OEIS complex, is a rare condition, comprised of severe congenital anomalies. This case report describes a 24-year-old 46,XY individual who had repair of the omphalocele at birth, but has remained with an unrepaired bl
Externí odkaz:
https://doaj.org/article/2371aaa236eb4fb48626ce685e15012a
Autor:
Lea A. Wehrli, Merlin Ariefdjohan, Jill Ketzer, Kristina Matkins, Luis De la Torre, Andrea Bischoff, Laura Judd-Glossy
Publikováno v:
Behavioral Sciences, Vol 14, Iss 5, p 379 (2024)
Background: Postoperative anal dilations (PAD) are the standard of care for patients after a posterior sagittal anorectoplasty (PSARP) for anorectal malformation (ARM) or a transanal pull-through (TP) procedure for Hirschsprung disease (HD). This stu
Externí odkaz:
https://doaj.org/article/ae84ec475dcc4eaf8fbf4d036e1390c1
Autor:
Lea A. Wehrli, Marina L. Reppucci, Jenny Stevens, Michael Arnold, Mark Lovell, María Zornoza, Andrea Bischoff, Luis De la Torre
Publikováno v:
Journal of Pediatric Surgery Open, Vol 3, Iss , Pp 100058- (2023)
Background: In Patients with Hirschsprung Disease (HSCR) suffering from obstructive symptoms after their pull-through surgery, a transition zone pull-through (TZPT) was suggested as a causing factor. Current guidelines recommend a reoperation resecti
Externí odkaz:
https://doaj.org/article/73d76f80bb0747ed826a4b1265a1ac97
Autor:
Kelly T. Harris, Daniel G. Pique, Lea A. Wehrli, Andrew Trecartin, Jonathan Roach, Naomi J. Meeks, Natalie J. Nokoff, Duncan T. Wilcox, Andrea Bischoff
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 95, Iss , Pp 102679- (2023)
Introduction: Here we report an infant with a 46,XY karyotype and novel de novo PPP1R12A stop-loss variant with a concomitant anorectal malformation (ARM) and difference in sex development (DSD). Case report: This is an infant born with ambiguous gen
Externí odkaz:
https://doaj.org/article/0a1621b6cf7044a285f88c537e66b74d
Autor:
Luis De-la Torre, Alfredo Domínguez, Michael Arnold, Mark Lovell, Diego Martínez, Andrea Bischoff, Lea Wehrli
Publikováno v:
Boletín Médico del Hospital Infantil de México, Vol 80, Iss 6 (2023)
Background: Surgeons create a neorectum to repair patients with Hirschsprung’s disease (HD), which should be formed from a normoganglionic bowel. However, the neorectum is occasionally created with a transition zone (TZ) bowel. A neorectum created
Externí odkaz:
https://doaj.org/article/5d9b4218a33f49d9853ae7e483d72d18
Publikováno v:
Urology Video Journal, Vol 13, Iss , Pp 100128- (2022)
Objective: A urogenital sinus (UGS) is a rare congenital condition defined by a common channel into which both the urinary and genital tracts drain. This malformation is often associated with other anomalies such as differences of sexual differentiat
Externí odkaz:
https://doaj.org/article/fb46a767578c45009bd9c244c1906857
Autor:
Laura A. Runck, Anna Method, Andrea Bischoff, Marc Levitt, Alberto Peña, Margaret H. Collins, Anita Gupta, Shiva Shanmukhappa, James M. Wells, Géraldine Guasch
Publikováno v:
Disease Models & Mechanisms, Vol 7, Iss 4, Pp 483-493 (2014)
Anorectal malformations are congenital anomalies that form a spectrum of disorders, from the most benign type with excellent functional prognosis, to very complex, such as cloaca malformation in females in which the rectum, vagina and urethra fail to
Externí odkaz:
https://doaj.org/article/11c84ea422d24ac19a3f1e9f3501380f
Autor:
J. Leslie Knod, Alexander J. Bondoc, Aaron P. Garrison, Andrea Bischoff, Belinda Dickie, Jason S. Frischer
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 3, Iss 11, Pp 499-500 (2015)
We describe two cases of concomitant Hirschsprung disease and esophageal atresia and tracheoesophageal fistula in the newborn, both of which were successfully diagnosed and managed in the neonatal period. This is the first report in the English liter
Externí odkaz:
https://doaj.org/article/bce7363c04b44cdcbf5ec46ed511b243