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Congenital lactase deficiency. 1966

F Lifshitz

UI MeSH Term Description Entries
D007223 Infant A child between 1 and 23 months of age. Infants
D007422 Intestines The section of the alimentary canal from the STOMACH to the ANAL CANAL. It includes the LARGE INTESTINE and SMALL INTESTINE. Intestine
D007785 Lactose A disaccharide of GLUCOSE and GALACTOSE in human and cow milk. It is used in pharmacy for tablets, in medicine as a nutrient, and in industry. Anhydrous Lactose,Lactose, Anhydrous
D007787 Lactose Intolerance The condition resulting from the absence or deficiency of LACTASE in the MUCOSA cells of the GASTROINTESTINAL TRACT, and the inability to break down LACTOSE in milk for ABSORPTION. Bacterial fermentation of the unabsorbed lactose leads to symptoms that range from a mild indigestion (DYSPEPSIA) to severe DIARRHEA. Lactose intolerance may be an inborn error or acquired. Lactose Malabsorption,Alactasia,Dairy Product Intolerance,Hypolactasia,Milk Sugar Intolerance,Intolerance, Lactose,Malabsorption, Lactose
D008297 Male Males
D002239 Carbohydrate Metabolism, Inborn Errors Dysfunctions of CARBOHYDRATE METABOLISM resulting from inborn genetic mutations that are inherited or acquired in utero. Carbohydrate Metabolism, Inborn Error
D004032 Diet Regular course of eating and drinking adopted by a person or animal. Diets
D005696 Galactosidases A family of galactoside hydrolases that hydrolyze compounds with an O-galactosyl linkage. EC 3.2.1.-. Galactosidase
D005951 Glucose Tolerance Test A test to determine the ability of an individual to maintain HOMEOSTASIS of BLOOD GLUCOSE. It includes measuring blood glucose levels in a fasting state, and at prescribed intervals before and after oral glucose intake (75 or 100 g) or intravenous infusion (0.5 g/kg). Intravenous Glucose Tolerance,Intravenous Glucose Tolerance Test,OGTT,Oral Glucose Tolerance,Oral Glucose Tolerance Test,Glucose Tolerance Tests,Glucose Tolerance, Oral
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man

Related Publications

F Lifshitz
Congenital and adult intestinal lactase deficiency.
May 1976, The New England journal of medicine,
F Lifshitz
[Congenital lactase deficiency: Identification of a new mutation].
May 2015, Anales de pediatria (Barcelona, Spain : 2003),
F Lifshitz
Intestinal beta-galactosidases in adult low lactase activity and in congenital lactase deficiency.
January 1974, Enzyme,
F Lifshitz
Four novel mutations in the lactase gene (LCT) underlying congenital lactase deficiency (CLD).
January 2009, BMC gastroenterology,
F Lifshitz
Impaired trafficking and subcellular localization of a mutant lactase associated with congenital lactase deficiency.
June 2009, Gastroenterology,
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Mutations in the translated region of the lactase gene (LCT) underlie congenital lactase deficiency.
February 2006, American journal of human genetics,
F Lifshitz
Congenital lactase deficiency. A clinical study on 16 patients.
April 1983, Archives of disease in childhood,
F Lifshitz
Hypercalcemia and nephrocalcinosis in patients with congenital lactase deficiency.
December 1995, The Journal of pediatrics,
F Lifshitz
[Lactase deficiency].
August 1974, Zeitschrift fur die gesamte innere Medizin und ihre Grenzgebiete,
F Lifshitz
[Lactase deficiency].
January 1966, Tijdschrift voor gastro-enterologie,
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