Literature DB >> 29502913

Inborn Errors of Metabolism with Cognitive Impairment: Metabolism Defects of Phenylalanine, Homocysteine and Methionine, Purine and Pyrimidine, and Creatine.

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.
Copyright © 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Creatine metabolism defects; Homocysteine methionine; Phenylalanine; Purine pyrimidine

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Substances:

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


  2 in total

Review 1.  Common metabolic disorder (inborn errors of metabolism) concerns in primary care practice.

Authors:  Marisha Agana; Julia Frueh; Manmohan Kamboj; Dilip R Patel; Shibani Kanungo
Journal:  Ann Transl Med       Date:  2018-12

2.  Blood levels of circulating methionine components in Alzheimer's disease and mild cognitive impairment: A systematic review and meta-analysis.

Authors:  Yan Zhao; Xinyi Dong; Bingyu Chen; Yizhou Zhang; Sijia Meng; Fangzhen Guo; Xiaojing Guo; Jialei Zhu; Haoyue Wang; Huixian Cui; Sha Li
Journal:  Front Aging Neurosci       Date:  2022-07-22       Impact factor: 5.702

  2 in total

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