Results 291 to 300 of about 829,213 (404)
Rapunzel syndrome: Trichobezoar‐induced pancreatitis unraveled
Abstract Trichobezoars are rare hair‐based intraluminal foreign bodies that may cause significant gastrointestinal complications, particularly when extending into the duodenum as in Rapunzel syndrome. We report the case of an 11‐year‐old girl with sensory processing difficulties and undiagnosed avoidant/restrictive food intake disorder (ARFID), who ...
Halen Scott +4 more
wiley +1 more source
Reconstruction of Iatrogenic Bile Duct Injuries following Laparoscopic Cholecystectomy. [PDF]
Hadi A, Khan I, Shah FO.
europepmc +1 more source
Abstract Pediatric B12 deficiency is most caused by insufficient dietary intake, malabsorption or autoimmune gastritis. We present a unique case of B12 deficiency in a pediatric patient with complex gastrointestinal anatomy and jejunal nutritional dependence nearly two decades after unsuccessful surgical intervention.
Angela H. Nguyen +2 more
wiley +1 more source
Evolving Strategies for the Optimal Management of Common Bile Duct Stones. [PDF]
Chon HK, Jo IH, Park CH.
europepmc +1 more source
Percutaneous transhepatic cholangiography rather than ultrasound as a screening test for postoperative biliary complications in liver transplant patients. [PDF]
Bron, KM +6 more
core
Abstract Objectives The American Academy of Pediatrics (AAP) Pediatrics Review and Education Program (PREP)® Gastroenterology (GI) Self‐Assessments help pediatric gastroenterologists and trainees prepare for subspecialty board exams by providing peer‐reviewed questions and critiques based on American Board of Pediatrics content specifications.
Annette G. Roberts +5 more
wiley +1 more source
Common bile duct stent-stone complex: the silent threat of forgotten biliary stents-case series. [PDF]
Parshaila R +4 more
europepmc +1 more source
Expanding the genotypic spectrum of PCSK1 deficiency: A novel mutation in severe neonatal diarrhea
Abstract Among congenital diarrhea and enteropathies (CODEs), proprotein convertase subtilisin/kexin type 1 (PCSK1) deficiency is a rare monogenic disorder, associated with severe neonatal diarrhea and polyendocrinopathies. We report an 18‐day‐old male neonate, born to consanguineous parents, presenting with persistent watery diarrhea, metabolic ...
Eleonora Saraceno +7 more
wiley +1 more source

