Results 41 to 50 of about 8,597 (234)

Duodenal duplication, intestinal malrotation and volvulus: An unusual cause of intestinal obstruction

Journal of Pediatric Surgery Case Reports, 2016
Duodenal duplication cysts are unusual congenital anomalies. Both intestinal malrotation and duodenal duplication may cause extrinsic duodenal obstruction.
Ivonete Siviero, Danielle Nunes Forny, Ivens Baker Méio, Claudia Renata Penna, Saulo Marcos Rebello Ferrante   +4 more
doaj   +1 more source

Newborn infants with bilious vomiting: a national audit of neonatal transport services [PDF]

, 2017
Objective: The precautionary approach to urgently investigate infants with bilious vomiting has increased the numbers referred to transport teams and tertiary surgical centres.
Budge, Helen, Kempley, Stephan, Leslie, Andrew, Mohinuddin, Syed, Ojha, Shalini, Ratnavel, Nanadiran, Sand, Laura, Sinha, Ajay   +7 more
core   +2 more sources

Fetal malrotation with midgut volvulus: Prenatal diagnosis and planning

Journal of Pediatric Surgery Case Reports, 2023
Introduction: Malrotation of the intestinal tract is a congenital malformation commonly found either incidentally or after affected individuals develop signs and symptoms of intestinal obstruction.
Oluyinka O. Olutoye II, J.D. Hammond II, Jamie Gilley, Ross M. Beckman, Marie Bulathsinghala, Sonya S. Keswani, Jonathan Davies, Mark V. Mazziotti, Roopali Donepudi, Michael A. Belfort, Alice King, Pamela M. Ketwaroo, Timothy C. Lee   +12 more
doaj   +1 more source

Duplication cyst mimicking intestinal malrotation with volvulus: A case report

Journal of Pediatric Surgery Case Reports, 2023
Introduction: Neonates presenting with bilious vomiting require emergent evaluation to rule out malrotation with volvulus. Enteric duplication cysts are congenital gastrointestinal lesions that can cause intestinal obstruction.
Matthew Ballweg, Patrick B. Thomas, Abdalla Zarroug, Angela, M. Hanna   +3 more
doaj   +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

Febrile status epilepticus and epileptogenesis: The FEBSTAT study

Epilepsia Open, EarlyView.
Abstract The multicenter FEBSTAT study (Consequences of Prolonged Febrile Seizures in Childhood: https://grantome.com/grant/NIH/R37‐NS043209‐12; PI S. Shinnar) examined the outcome of febrile status epilepticus (FSE) in over 200 prospectively enrolled infants, with many followed for 10 years after FSE.
Darrell V. Lewis, Douglas R. Nordli Jr., Douglas R. Nordli III, Shlomo Shinnar, Stephen Chan, Jacqueline A. Bello, L. Matthew Frank, James Voyvodic, William Gallentine, Syndi Seinfeld, Yoshimi Sogawa, Erica Weiss, David Masur, Yuan Xu, Solomon L. Moshé   +14 more
wiley   +1 more source

Hirschsprung disease and intestinal malrotation: A rare association with unique perioperative considerations

Journal of Pediatric Surgery Open, 2023
Background: Multiple etiologies exist for neonatal intestinal obstruction with similar presenting symptoms. While single etiology is the most common cause, concomitant surgical diagnoses exist requiring unique peri‑operative considerations.
Dimitra M. Lotakis, Sydni Imel, Jack P. Vernamonti, Brianna L. Spencer, Matthew W. Ralls   +4 more
doaj   +1 more source

Clinical, manometric, genetic, and histologic associations in pediatric intestinal pseudo‐obstruction: A case series

Journal of Pediatric Gastroenterology and Nutrition, EarlyView.
Abstract Objectives Pediatric intestinal pseudo‐obstruction (PIPO) is a severe bowel motility disorder characterized by impaired propulsion of gastrointestinal contents without mechanical obstruction. PIPO encompasses congenital and acquired disorders, including neuropathies, myopathies, and mesenchymopathies.
Sharon Wolfson, Myra Butrviengpunt, Naomi Tjaden, Alain J. Benitez, Archana S. Kota, Jennifer Webster, Prasanna Kapavarapu, Hayat Mousa, Robert O. Heuckeroth   +8 more
wiley   +1 more source

A case of split notochord syndrome: a child with a neuroenteric fistula presenting with meningitis [PDF]

, 2006
The authors describe a case of split notochord syndrome with a neuroenteric fistula in a newborn presenting with meningitis. Associated anomalies included agenesis of the corpus callosum, short colon, malrotation, epispadias, and an abnormally high ...
Lequin, M.H. (Maarten), Mancini, G.M.S. (Grazia), Ramshorst, G.H. (Gabrielle) van, Ven, C.P. (Cees) van de   +3 more
core   +1 more source

Expanding the genotypic spectrum of PCSK1 deficiency: A novel mutation in severe neonatal diarrhea

JPGN Reports, EarlyView.
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, Angelo Corso Faini, Silvia Deaglio, Marianna Pellegrini, Raffaele Buganza, Francesca Giuliani, Pier Luigi Calvo, Michele Pinon   +7 more
wiley   +1 more source