Results 111 to 120 of about 172,684 (393)
Advances in prognostic biomarkers for biliary atresia: Current insights and future directions
Abstract Biliary atresia (BA) is a progressive, fibrosing cholangiopathy of infancy characterized by inflammatory obstruction of the bile ducts, ultimately leading to end‐stage liver disease if untreated. Early diagnosis and timely surgical intervention via hepatoportoenterostomy (HPE) are critical for improving outcomes; however, prognostication ...
Ahmad Anouti+6 more
wiley +1 more source
La ascitis fetal aislada es una entidad asociada a múltiples patologías, el diagnostico se realiza usualmente cuando fueron descartados las otras causas de ascitis fetal.
Patricio Valdés+3 more
doaj
Biliary atresia: Where do we stand now?
The pathway from clinical suspicion to establishing the diagnosis of biliary atresia in a child with jaundice is a daunting task. However, investigations available help to point towards the correct diagnosis in reasonable time frame.
K. Govindarajan
semanticscholar +1 more source
Abstract Objectives Limited literature exists on non‐clinically significant varices (nCSV) and progression in children with portal hypertension (PHT). This study investigates trends and associations in this cohort. Methods This retrospective cohort study analysed 70 children with nCSV undergoing surveillance endoscopy between January 2012 and 2024 ...
Cody Chan+6 more
wiley +1 more source
Combined Duodenal Atresia and Pure Esophageal Atresia [PDF]
Duodenal atresia is not an uncommon congenital anomaly, occurring in 1 in 6,000 to 1 in 10,000 live births [1]; it is also frequently associated with trisomy 21, which carries a high rate of congenital heart defects. On the other hand, pure esophageal atresia alone is rare, occurring in 1 in 36,000 births [2].
openaire +2 more sources
Abstract Objectives European Society for Pediatric Gastroenterology, Hepatology, and Nutrition (ESPGHAN) guidelines recommend first‐line serology for suspected celiac disease (CeD), measuring only transglutaminase antibodies (TGA‐immunoglobulin A [IgA]) plus total IgA.
Anna Litwin+11 more
wiley +1 more source
An antenatal diagnosis: Congenital high airway obstruction
Congenital high airway obstruction (CHAOS) is a rare lethal fetal malformation characterised by obstruction to the fetal upper airway, which can be partial or complete. Antenatal diagnosis of CHAOS is important due to recent management options. Diagnosis
S Miital+4 more
doaj +1 more source
Transplantation in children [PDF]
Kidney transplantation in very young children, less than 2 years of age, has usually failed, mainly because of difficulties maintaining these patients on hemodialysis long enough to permit retransplantation after loss of the original graft.
Charles W. Putnam+15 more
core +1 more source
Abstract Objectives Development of necrotizing enterocolitis (NEC) in infants with complex congenital heart disease (CHD) has serious negative clinical outcomes. Unfortified expressed breast milk (EBM) is this high‐risk population's enteral feed of choice. EBM often requires fortification to meet nutritional needs to prevent malnutrition.
Jemma Woodgate+7 more
wiley +1 more source
Case report: Isolated unilateral pulmonary vein atresia diagnosed on 128-slice multidetector CT
Unilateral pulmonary venous atresia is an uncommon entity that is generally believed to be congenital. Most patients present in infancy or childhood with recurrent chest infections or hemoptysis.
Rashmi Dixit+4 more
doaj +1 more source