| Literature DB >> 29502913 |
Evgenia Sklirou1, Uta Lichter-Konecki2.
Abstract
Phenylketonuria is a defect in phenylalanine metabolism resulting in the excretion of phenylketones and severe intellectual disability. The principle of eliminating the offending amino acid from the diet as a successful treatment strategy was demonstrated. The development of a low methionine diet to treat homocystinuria was established after identifying the transsulfuration pathway resulting in cysteine synthesis. Both conditions are examples of disorders of amino acid metabolism. Lesch-Nyhan syndrome, a rare disorder of purine metabolism resulting in intellectual disability and self-injurious behavior, is a classical inborn error of metabolism. Disorders of creatine biosynthesis are relatively newly described and less known diseases.Entities:
Keywords: Creatine metabolism defects; Homocysteine methionine; Phenylalanine; Purine pyrimidine
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Year: 2018 PMID: 29502913 DOI: 10.1016/j.pcl.2017.11.009
Source DB: PubMed Journal: Pediatr Clin North Am ISSN: 0031-3955 Impact factor: 3.278