Results 111 to 120 of about 88,904 (264)

Maralixibat for the treatment of severe xanthomas in two children with Alagille syndrome: Case reports

open access: yesJPGN Reports, EarlyView.
Abstract Alagille syndrome (ALGS) is a rare, autosomal dominant disorder which presents with a broad range of clinical manifestations, including cholestatic pruritus. A unique manifestation of ALGS is the presence of xanthomas in 24%–42% of patients, which can lead to liver transplantation.
Geetanjali Bora   +2 more
wiley   +1 more source

A rare cause of upper gastrointestinal bleeding

open access: gold, 2016
Mahir Gachabayov, Petr Mityushin
openalex   +1 more source

Rapunzel syndrome: Trichobezoar‐induced pancreatitis unraveled

open access: yesJPGN Reports, EarlyView.
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

Sentinel events in pediatric hepatology: A pilot simulation curriculum

open access: yesJPGN Reports, EarlyView.
Abstract Objectives Sentinel hepatology events require robust prior experience to accurately diagnose and manage. Given the rarity of complex pediatric liver disease, gastroenterology (GI) fellows do not uniformly get exposure to these patients.
Anne Lyon   +7 more
wiley   +1 more source

PTH-44 Improving the Morecambe Bay Acute Upper Gastrointestinal Bleeding Service [PDF]

open access: gold, 2021
Christopher Mysko   +4 more
openalex   +1 more source

Gastric antral vascular ectasia: A rare etiology of gastrointestinal bleeding in children

open access: yesJPGN Reports, EarlyView.
Abstract Gastrointestinal bleeding is relatively common in children. While most patients present with mild bleeding, gastric antral vascular ectasia (GAVE) is a rare but potentially life‐threatening cause. GAVE is typically associated with chronic conditions and more common in adults.
Omar Alharbi   +3 more
wiley   +1 more source

Menetrier's: A pediatric chronic state of disease with a possible heritable form

open access: yesJPGN Reports, EarlyView.
Abstract Menetrier's disease (MD) is a rare, typically transient, hypertrophic gastropathy with under 1000 adult cases and 50 pediatric cases known worldwide. Pediatric cases most often present with an infectious etiology. We present a case of a teenage male expressing a chronic state of disease without infectious origin.
MariaElena Terzis   +2 more
wiley   +1 more source

Juvenile polyposis in a SMAD4‐mutated child: A call for early surveillance

open access: yesJPGN Reports, EarlyView.
Abstract We report the case of a 10‐year‐old boy with hereditary hemorrhagic telangiectasia (HHT) and a family history of SMAD4‐related juvenile polyposis syndrome (JPS), presenting with hypoferritinaemia unresponsive to oral supplementation. Endoscopic evaluation revealed multiple gastrointestinal polyps, including duodenal, gastric, and colonic ...
Claudia Lorusso   +10 more
wiley   +1 more source

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