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Intestinal malrotation: case description and publication analysis

open access: yesВестник медицинского института «Реавиз»: Реабилитация, врач и здоровье, 2023
Intestinal malrotation is a rare congenital anatomical anomaly that results from an abnormal bowel rotation at 10–12 weeks of embryonic development. Clinical manifestations depend on age.
M. V. Simonov   +3 more
doaj   +1 more source

IMPOWER: a national patient-generated registry for intestinal malrotation exploring diagnosis, treatment, and surgical outcomes

open access: yesOrphanet Journal of Rare Diseases, 2023
Background Intestinal malrotation is a rare congenital condition with potentially devastating consequences due to potential volvulus and massive intestinal necrosis.
Sydney A. Martinez   +7 more
doaj   +1 more source

CONGENITAL INTESTINAL MALROTATION IN ADULT PATIENTS [PDF]

open access: yesBasrah Journal of Surgery, 2020
Congenital intestinal malrotation is an impaired embryological development of the gut causing incomplete rotation and attachment of the intestines to the abdominal wall.
Firas Jabir   +3 more
doaj   +1 more source

Intestinal malrotation in a patient who underwent radical cystectomy and ileal conduit construction: A case report

open access: yesUrology Case Reports, 2020
A 74-year-old male underwent laparoscopic radical cystectomy for invasive bladder cancer with open surgery for lymph node dissection and urinary diversion (ileal conduit).
Fumito Yamabe   +5 more
doaj   +1 more source

Acute jaundice as a manifestation of midgut volvulus in a 6-year-old child: A case report

open access: yesJournal of Pediatric Surgery Case Reports, 2023
Introduction: Midgut malrotation is a congenital anomaly characterized by the incomplete rotation of the midgut during embryonic development. Although often asymptomatic, midgut malrotation can lead to complications such as midgut volvulus.
Ali Alakbar Nahle   +6 more
doaj   +1 more source

Novel abdomino-pelvic anomalies in Kagami-Ogata syndrome

open access: yesJournal of Pediatric Surgery Case Reports, 2021
Kagami-Ogata syndrome (KOS) is a rare genomic imprinting disorder of chromosome 14 with characteristic facial features, a small, bell-shaped thorax, muscular hypotonia, and abdominal wall defects.
Kelly Lamiman   +8 more
doaj   +1 more source

Mesenteric cyst as a presentation of chronic midgut volvulus in a 12 year old boy

open access: yesJournal of Pediatric Surgery Case Reports, 2020
Intestinal malrotation is a congenital anomaly of intestinal rotation and fixation that is generally symptomatic in the neonatal population. However, malrotation in an important minority is diagnosed long after infancy and is not manifested by the ...
E. Botchway, N. Tshifularo, M.J. Human
doaj   +1 more source

Atypical presentation of concurrent duodenal web and malrotation

open access: yesJournal of Pediatric Surgery Case Reports, 2020
Intestinal malrotation in neonates is well known with incidence of 1:500 and symptomatic incidence 1:6000 births. Duodenal web as a cause of intestinal obstruction is less common with incidence of 1:10000–1:40000.
Sajad Ahmad Wani   +3 more
doaj   +1 more source

Delayed laparoscopic cholecystectomy in a case of acute cholecystitis and intestinal malrotation type I

open access: yesClinics and Practice, 2019
In adults, intestinal malrotation is an oligosymptomatic entity that is occasionally discovered during the course of diagnostic studies for other causes.
Ana Arias   +5 more
doaj   +1 more source

Gastroschisis with malrotation, gut duplication and Meckel's diverticulum; a rare association

open access: yesJournal of Pediatric Surgery Case Reports, 2021
Gastroschisis is defined as a congenital anterior abdominal wall defect which is rarely associated with other congenital anomalies. Gastrointestinal anomalies are the most common associations including malrotation.
Ahmed Elrouby, MD, Ahmed Maher, MS
doaj   +1 more source

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