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Pediatric and Adult Nutrition in Chronic Diseases, Developmental Disabilities, and Hereditary Metabolic DisordersPrevention, Assessment, and Treatment$
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Shirley W. Ekvall and Valli K. Ekvall

Print publication date: 2017

Print ISBN-13: 9780199398911

Published to Oxford Scholarship Online: April 2017

DOI: 10.1093/acprof:oso/9780199398911.001.0001

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PRINTED FROM OXFORD SCHOLARSHIP ONLINE (www.oxfordscholarship.com). (c) Copyright Oxford University Press, 2018. All Rights Reserved. Under the terms of the licence agreement, an individual user may print out a PDF of a single chapter of a monograph in OSO for personal use (for details see www.oxfordscholarship.com/page/privacy-policy).date: 20 November 2018

Glutaric Acidemia Type I

Glutaric Acidemia Type I

Chapter:
(p.311) 44 Glutaric Acidemia Type I
Source:
Pediatric and Adult Nutrition in Chronic Diseases, Developmental Disabilities, and Hereditary Metabolic Disorders
Author(s):

Dianne Frazier

Publisher:
Oxford University Press
DOI:10.1093/acprof:oso/9780199398911.003.0044

This chapter discusses glutaric acidemia type I, including clinical features, biochemical abnormalities, factors to be considered in nutritional evaluation and treatment, dietary treatment, and monitoring.

Keywords:   Glutaric acidemia type 1, glutaric acid, extrapyramidal movements, clinical features, biochemical abnormalities, dietary treatment

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