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The definition of early allograft dysfunction (EAD) varies, and has hardly been studied in pediatric transplantation (pLT) since the adult EAD...
Necrotizing enterocolitis (NEC) and spontaneous intestinal perforation (SIP) lead to significant morbidity and mortality in extreme-low birth...
Hereditary Spherocytosis (HS) is a common genetic hematological disorder causing a life-long hemolytic anemia, with sequela of hemolysis. Children...
Canada's Royal College of Physicians and Surgeons established a competency-based medical education (CBME) training in pediatric surgery in 2021....
Mowat-Wilson Syndrome (MWS) is a rare autosomal dominant genetic disorder. Approximately half of individuals with MWS present with Hirschsprung's...
Hypertrophic pyloric stenosis (HPS) is an acquired condition that causes gastric outlet obstruction in infants and requires operative treatment....