Zobrazeno 1 - 10
of 641
pro vyhledávání: '"Anorectal anomalies"'
Publikováno v:
National Board of Examinations Journal of Medical Sciences, Vol Volume 2, Iss 3, Pp 168-191 (2024)
Normally, at birth, females have separate perineal orifices for the urinary, reproductive and digestive tracts, while males have individual openings for the urogenital and digestive tracts. However, during fetal development, both sexes pass through a
Externí odkaz:
https://doaj.org/article/17203435d5e54d51a4d8e912788561ae
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 78, Iss , Pp 102185- (2022)
Currarino syndrome is a rare congenital malformation characterised by the triad of: an anorectal malformation, sacral bony defect and presacral mass. One rare but possible anorectal malformation is an anal canal duplication, a congenital anomaly whic
Externí odkaz:
https://doaj.org/article/fdd013002588473bb2ac43527191bd1c
Akademický článek
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Publikováno v:
African Journal of Paediatric Surgery, Vol 14, Iss 2, Pp 27-31 (2017)
Background: Rectovestibular fistula (RVF) is the most common type of anorectal malformations in females. The need for a diverting colostomy during correction of defect has ignited a heated debate. In this study, we reviewed the girls with RVF that ha
Externí odkaz:
https://doaj.org/article/d80269bf37da4a92a3bf033e6fa98cc5
Publikováno v:
Journal of Pediatric Surgery. 57:314-321
The operations involved in the repair of complete bladder exstrophy (CBE), familiarly known as the Kelly procedure, evolved over more than 100 years. Through repeated cycles of trial and error, some of the most prominent urologists in the world devel
Autor:
Rashid V. Halafov, Olga G. Mokrushina, Lubov V. Petrova, Svetlana K. Emirbekova, Marina V. Levitskaya, Madina A. Chundokova, Olga V. Koshko, Vasiliy S. Shumikhin, Julia V. Shugina
Publikováno v:
Russian Journal of Pediatric Surgery, Anesthesia and Intensive Care. 11:315-324
BACKGROUND: The preserved cloaca is a particular type of anorectal anomaly. The combination of urological, genital, and rectal abnormalities makes radical reconstruction difficult. MATERIALS AND METHODS: This study examined operations performed in 50
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 22, Iss 1, Pp 1-6 (2021)
Background Anorectal malformations (ARM) represent a wide spectrum of defects. Caudal and genitourinary malformations can associate with anorectal malformations. Genetic factors may play role in the development of anorectal malformations. Perineal ma
Publikováno v:
Journal of Pediatric Surgery. 56:1570-1575
Background Anorectal anomalies (ARA) are characterized by different clinical presentations in both sexes with consequently different management protocols. There exist several controversies and different strategies to manage ARA in the female. Purpose
Publikováno v:
Annals of Pediatric Surgery, Vol 17, Iss 1, Pp 1-7 (2021)
Background Redo surgery for anorectal anomalies (ARA) may be considered a special category of reconstructive surgery with less predictable outcomes. In this report, we studied anatomical derangements in a group of boys following a previously complica
Autor:
Krishna Mohan Medicherla, Ashwani Kumar Mishra, Sonal Gupta, Praveen Mathur, Prashanth Suravajhala
Publikováno v:
Children; Volume 10; Issue 5; Pages: 902
Anorectal malformations (ARM) are individually common, but Congenital Pouch Colon (CPC) is a rare anorectal anomaly that causes a dilated pouch and communication with the genitourinary tract. In this work, we attempted to identify de novo heterozygou