Amino acid metabolism disorders.
- Author:
Dong Hwan LEE
1
Author Information
1. Department of Pediatrics, College of Medicine, Soonchunhyang University, Korea. ldh@hosp.sch.ac.kr
- Publication Type:Review
- Keywords:
Amino acid metabolism;
Phenylketonuria;
Urea cycle defects;
Maple syrup urine disease;
Homocystinuria
- MeSH:
Amino Acids;
Brain;
Compensation and Redress;
Cytosol;
Homocystinuria;
Infant, Newborn;
Kidney;
Liver;
Maple Syrup Urine Disease;
Metabolism*;
Neonatal Screening;
Phenylketonurias;
Plasma;
Trace Elements
- From:Hanyang Medical Reviews
2005;25(3):65-78
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Deficiencies of enzymes involved in amino acid metabolism frequently result in accumulation of toxic substances and subsequent organ damage. The brain, liver and kidneys are the most frequently affected organs. Acute symptoms are often associated with catabolic states that lead to the breakdown of endogenous proteins and the release of large amounts of amino acids. The clinical features result from the toxicity of the deficiency, and the extent of protein intake or endogenous amino acid release in protein compensation. Many disorders of this group are recognised by neonatal screening with tandem MS. Most aminoacidopathies are caused by deficiencies of cytosolic enzymes and are recognised by amino acid analysis in plasma (or urine). Treatment usually involves(a) protein restriction, (b) supplementation of amino acids with unimpaired metabolism as well as trace elements, and (c) specific measures for detoxification if indicated. Treatment is not restricted to childhood but usually must be continued throughout life.
