Results 51 to 60 of about 35,475 (152)

Combined duodenal and jejunal atresia forming a bile filled cyst, presenting as an abdominal mass: A case report and review of the literature

open access: yesJournal of Pediatric Surgery Case Reports, 2015
The simultaneous occurrence of duodenal and jejunoileal atresia in the newborn is very rare. This is not surprising considering the unrelated embryogenesis behind the development of the two congenital anomalies.
Ahmad Zaghal   +2 more
doaj   +1 more source

Intestinal Atresia: Twenty Years of Experience at a Reference Hospital

open access: yesİstanbul Medical Journal, 2021
Introduction:The aim of this study was to reveal the factors that affect the clinical outcomes of patients undergoing surgery in our university hospital for intestinal atresia (IA) and to share our experience.Methods:We analyzed data from 74 newborns ...
Mehmet Saraç   +5 more
doaj   +1 more source

Analysis of Prevalence and Mortality Among Neonates and Children With Intestinal Atresia: A Multinational Study, 1974–2015

open access: yesBirth Defects Research, Volume 118, Issue 4, April 2026.
ABSTRACT Introduction Small intestinal atresia (SIA) consists of a congenital obstruction of the lumen of the duodenum, jejunum, or ileum with varying severity. The aim of the investigation was to analyze the prevalence and mortality of SIA, using data from the International Clearinghouse for Birth Defects Surveillance and Research (ICBDSR).
Angie Carreño   +29 more
wiley   +1 more source

Serum aspartate aminotransferase to platelet ratio index in relation to liver histopathology of biliary atresia

open access: yesJournal of Pediatric Gastroenterology and Nutrition, Volume 82, Issue 4, Page 929-938, April 2026.
Abstract Objectives To investigate the prognostic significance of aspartate aminotransferase to platelet ratio index (APRI) in relation to histopathological features across the clinical course of biliary atresia (BA). Methods In this observational cohort study, we enrolled 135 BA patients with available APRI values at Kasai portoenterostomy (KPE, n ...
Nicholas Nordenheim   +7 more
wiley   +1 more source

Challenging management of a baby with congenital multiple intestinal atresia, trisomy 18 and extremely low birth weight: a case report

open access: yesSurgical Case Reports, 2023
Background Extremely low birth weight (
Mitsumasa Okamoto   +6 more
doaj   +1 more source

Vitamin B12 deficiency in a pediatric patient with gastric obstruction and jejunal feeding dependence: A case report

open access: yesJPGN Reports, Volume 7, Issue 1, Page 174-178, February 2026.
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

Intestinal and Multivisceral Transplantation: Where We Stand Today

open access: yesPediatric Transplantation, Volume 30, Issue 1, January 2026.
ABSTRACT Intestinal and multivisceral transplantation has evolved from an experimental to a life‐saving procedure for children and adults with complications of gut failure (GF). Suboptimal long‐term outcomes of transplant elicit recent advances in surgical and medical gut rehabilitation along with the introduction of glucagon‐like peptide‐2 (GLP‐2 ...
Mohamed Maklad   +5 more
wiley   +1 more source

Apple-Peel Intestinal Atresia Along with Isolated Jejunal Duplication Cyst in a Newborn – An Extremely Rare Case Report and Brief Review [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2017
Apple-peel type of intestinal atresia and non-communicating jejunal duplication cyst are rare congenital malformations. The coexistence is not reported in English literature.
Prasanta Kumar Tripathy   +3 more
doaj   +1 more source

Manganese Supplements and Dystonia

open access: yesPediatric Neurology Briefs, 1995
A 7 month old girl who developed dystonic movements of the arms after a 3 month period of parental nutrition for jejunal atresia and bowel resection is reported from Great Ormond Street Hospital, London, UK.
J Gordon Millichap
doaj   +1 more source

Genotype–Phenotype Correlation in TTC7A ‐Associated Gastrointestinal Defects and Immunodeficiency Syndrome 1

open access: yesAmerican Journal of Medical Genetics Part A, Volume 197, Issue 12, December 2025.
ABSTRACT Gastrointestinal defects and immunodeficiency syndrome 1 (GIDID1) is a rare autosomal recessive disorder caused by biallelic variants in TTC7A. GIDID1 is characterized by a broad clinical spectrum ranging from very early‐onset inflammatory bowel disease (VEOIBD) to multiple intestinal atresia (MIA) with or without immunological manifestations.
Julia Imhoff   +8 more
wiley   +1 more source

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