Lactose intolerance: diagnosis, genetic, and clinical factors
- PMID: 22826639
- PMCID: PMC3401057
- DOI: 10.2147/CEG.S32368
Lactose intolerance: diagnosis, genetic, and clinical factors
Abstract
Most people are born with the ability to digest lactose, the major carbohydrate in milk and the main source of nutrition until weaning. Approximately 75% of the world's population loses this ability at some point, while others can digest lactose into adulthood. This review discusses the lactase-persistence alleles that have arisen in different populations around the world, diagnosis of lactose intolerance, and its symptomatology and management.
Keywords: LCT gene; MCM6 gene; hypolactasia; lactase non-persistence; lactase persistence; lactose.
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LCT-13910C>T;
LCT-22018G>A/-13910CC;
LCT-13915T>G;
LCT-14010G>C;
LCT-13907C>G.References
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