Results 41 to 50 of about 896,464 (230)
Diagnostic possibilities of lactase deficiency in children with cystic fibrosis
Introduction. Children with cystic fibrosis often have gastrointestinal symptoms despite properly selected primary therapy and pancreatic substitution therapy. A possible reason is lactase deficiency.
E. Roslavtseva +7 more
semanticscholar +1 more source
Today, the violations of the digestive system in children of the first years of life remain the actual problem of practical pediatrics and are the common cause for parents to visit a doctor.
R.V. Tkach +3 more
doaj +1 more source
The use of lactase in the relief of chronic diarrhea syndrome in children
The article deals with one of the most urgent problems of pediatrics — malassimilation syndrome due to lactose intolerance in children at different age periods.
L.G. Voloshyna +10 more
doaj +1 more source
Disaccharidase deficiency and functional bowel diseases [PDF]
Aim. To elucidate the role of intestinal carbohydrases (glucoamylase, maltase, sucrose, and lactase) in the etiology and pathogenesis of functional bowel diseases (FBD). Subjects and methods. 74 patients (36 men and 38 women) aged 18 to 50 years with FBD
A I Parfenov +6 more
doaj +1 more source
Laboratory signs of carbohydrate malabsorption in early age children with rotavirus infection
The aim – to determine the laboratory manifestations of carbohydrate malabsorption syndrome in the dynamics of rotavirus infection in early age children and to identify the factors that influence its severity. Materials and methods. The study included
N. V. Vorobiova, O. V. Usachova
doaj +1 more source
Novel Role of Gut-Derived Roseburia Intestinalis in Safeguarding Intestinal Barrier Integrity and Microenvironment Homeostasis During Arsenic Exposure. [PDF]
Arsenic exposure disrupts intestinal barriers and gut microenvironment. Fecal microbiota transplantation (FMT) alleviates arsenic‐induced damage, with gut‐derived Roseburia intestinalis (R.i) identified as a key protective strain. R.i administration counters arsenic toxicity through immunomodulatory pathways and metabolites.
Zhou L +15 more
europepmc +2 more sources
Congenital lactase deficiency (CLD) is a rare autosomal recessive genetic disorder, leading to a dysfunctional lactase‐phlorizin hydrolase (LPH). LPH is a ß‐galactosidase located in the intestinal brush border membrane and indispensable for lactose ...
Lara M. Marten +3 more
semanticscholar +1 more source
Lactose is the main carbohydrate in human and mammalian milk. Lactose requires enzymatic hydrolysis by lactase into D-glucose and D-galactose before it can be absorbed.
Ralf G. Heine +9 more
doaj +3 more sources
A modern problem of practical pediatrics is secondary lactase deficiency - intolerance to dairy products containing lactose, which develops in response to a decrease in lactase activity due to enterocyte damage in an infectious, allergic, or other ...
Y. Marushko +4 more
semanticscholar +1 more source
PERCC1‐associated enteropathy: Diagnostic challenges and enteral autonomy achieved with teduglutide
Abstract Congenital diarrheas and enteropathies (CODE) are rare inherited disorders characterized by early‐onset intractable diarrhea. Though progress has been made in elucidating the genetic basis of CODE, much remains to be discovered. Another challenge is the lack of curative therapies—treatment is primarily supportive including enteral and ...
Angela Tran, Vivien Nguyen, Phuong Huynh
wiley +1 more source

