Results 61 to 70 of about 7,885 (252)

بررسی مشکلات تشخیصی مالروتاسیون در 11 بیمار با تظاهرات مزمن [PDF]

, 2007
زمینه و هدف: مالروتاسیون روده به طور معمول در اولین ماه‌های زندگی تظاهر می‌کند ولی گاهی ممکن است در مراحل بعدی زندگی تظاهر نماید که باعث روند دشوارتر تشخیص و اشتباهات احتمالی می‌شود.
خورگامي, ژامك, نحـوي, هدايت‌اله   +1 more
core  

Extremely Rare Neonatal Case With Pyloric Atresia, Heart Defects, Hypotonia, Jaundice, and Acidosis

Clinical Case Reports, Volume 13, Issue 8, August 2025.
ABSTRACT Pyloric atresia (PA) is an exceptionally rare congenital cause of gastric outlet obstruction, often associated with syndromic conditions such as epidermolysis bullosa (EB). This case highlights a diagnostically challenging presentation of *non‐syndromic pyloric atresia* in a neonate, complicated by a moderate mid‐muscular ventricular septal ...
Saja Abouodeh, Yasmeen Alshami, Osama Hroub, Mohammad Hroub, Ahmad G. Hammouri, Ahmad Shaltaf, Wafa Shihadeh, Nimatee Dawod   +7 more
wiley   +1 more source

Atypical presentation of concurrent duodenal web and malrotation

Journal 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, Kumar Abdul Rashid, Kartic Saxena, Mahim Khan   +3 more
doaj  

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

Journal 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  

A Rare Case of Ileal Intussusception Caused by Primary Small Bowel Trichobezoar and Meckel's Diverticulum in an Autistic Child

Clinical Case Reports, Volume 13, Issue 8, August 2025.
ABSTRACT Intussusception is a condition in which one part of the intestine slides into an adjacent part of the intestine. Intussusception is an important cause of an acute abdomen and the second most common cause of bowel obstruction in children.
Marwa Messaoud, Habib Ullah Joya, Amani N. Alansari, Abir Jouini, Amine Ksiaa, Ahmed Zrig, Lasaad Sahnoun   +6 more
wiley   +1 more source

Chronic Intussusception Associated with Malrotation in a Child: A Variation of Waugh’s Syndrome?

Case Reports in Surgery, 2016
Chronic intussusception is a relatively uncommon disease most commonly observed in older children. Waugh’s syndrome represents a rare entity characterized by intestinal malrotation and acute intussusception.
Nick Zavras, Konstantinos Tsilikas, George Vaos   +2 more
doaj   +1 more source

Heterotaxy syndrome with intestinal malrotation, polysplenia and azygos continuity

Clinics and Practice, 2018
Heterotaxy syndrome is a situs anomaly that comprises a large spectrum of cardiac and extracardiac malformations. Its association with intestinal malrotation is frequent. This later might be asymptomatic or manifest by signs of abdominal discomfort or of
Stéphanie Cupers, Christine Van Linthout, Brigitte Desprechins, Léon Rausin, Martine Demarche, Marie-Christine Seghaye   +5 more
doaj   +1 more source

Pancreaticoduodenectomy with malrotation following reoperation due to torsion of efferent loop: a case report

Surgical Case Reports, 2020
Background Malrotation is a congenital anomaly during the development of the embryonic intestine. Although it is generally considered a pediatric surgical condition, it can have significant implications for adult surgery in terms of reconstruction.
Yumiko Kageyama, Ryuzo Yamaguchi, Shinya Watanabe, Keiji Aizu, Shinichiro Kobayashi, Fumiya Sato, Hironori Fujieda, Yoshitaka Toyoda, Tsutomu Iwata   +8 more
doaj   +1 more source

Wilms Tumor in Children With AMER1/WTX Germline Pathogenic Variants: A Multicenter Case Series

Pediatric Blood &Cancer, Volume 72, Issue 8, August 2025.
ABSTRACT Background 10–15% of children with Wilms tumor (WT) have predisposing genetic syndromes. Somatic mutations are frequently identified; however, germline pathogenic variants in AMER1 are much less prevalent and are associated with osteopathia striata with cranial sclerosis (OSCS).
Insiyah Campwala, Jaclyn Schienda, Andrew J. Murphy, Basil Hashimi, Taylor Perry, Nicholas Cost, Junne Kamihara, Elizabeth A. Mullen, Teresa Santiago, Marcus M. Malek   +9 more
wiley   +1 more source

Investigation of chronic diarrhoea in infancy. [PDF]

, 2013
Diarrhoea in infants and young children is defined as >200g/day of stools, and occurs when there is an imbalance between intestinal fluids absorption and secretion.
BERNI CANANI, Roberto, Cosenza, L, De Martino, L, Passariello, Annalisa, Pezzella, V, Terrin, Gianluca   +5 more
core   +1 more source