Disaccharidase deficiency.

The American journal of clinical nutrition ·Vol. 22 ·No. 2 ·1969-02-00 ·Pages 181-90

Bayless TM, Christopher NL

Abstract

暂无摘要

Keywords

Age Factors Biology Carbohydrate Metabolic Effects Cultural Background Demographic Factors Diseases Ethnic Groups Literature Review Metabolic Effects Nutrition Disorders--etiology Physiology Population Population Characteristics

MeSH Terms

Adolescent Adult Carbohydrate Metabolism, Inborn Errors/etiology Disaccharides/metabolism Galactose Glucose Glycoside Hydrolases Humans Intestinal Absorption Lactose Intolerance Metabolic Diseases Nutritional Physiological Phenomena Sucrose

Chemicals

Disaccharides Sucrose Glycoside Hydrolases Glucose Galactose

Authors & Affiliations

2 authors, click to expand affiliations / ORCID

Bayless T M

Christopher N L

Other Abstracts

eng

This review of the literature and current knowledge concerning a nutritional disorder of disaccharidase deficiency discusses the following topics: 1) a description of disorders of disaccharide digestion

2) some historical perspective on the laboratory and bedside advances in the past 10 years that have helped define a group of these digestive disorders

3) a classification of conditions causing disaccharide intolerance

and 4) a discussion of some of the specific clinical syndromes emphasizing nutritional consequences of these syndromes. The syndromes described include congenital lactase deficiency, acquired lactase deficiency in teenagers and adults, acquired generalized disaccharidase deficiency secondary to diffuse mucosal damage, acquired lactose intolerance secondary to alterations in the intestinal transit, sucrase-isomaltase deficiencies, and other disease associations connected with lactase deficiency such as colitis.

Article Info

Journal

The American journal of clinical nutrition

Abbr.

Am J Clin Nutr

ISSN

0002-9165

DOI

10.1093/ajcn/22.2.181

Published

1969-02-00

Pages

181-90

Language

English

Region

United States

NLM ID

0376027

Subset

External Links

PubMed source DOI: 10.1093/ajcn/22.2.181 View journal details

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Disaccharidase deficiency.

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