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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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Fragile X Syndrome

Fragile X Syndrome

Chapter:
(p.373) 56 Fragile X Syndrome
Source:
Pediatric and Adult Nutrition in Chronic Diseases, Developmental Disabilities, and Hereditary Metabolic Disorders
Author(s):

Tori L. Schaefer

David L. Nelson

Craig A. Erickson

Publisher:
Oxford University Press
DOI:10.1093/acprof:oso/9780199398911.003.0056

This chapter discusses fragile X syndrome, including prevalence, phenotype and clinical abnormalities, molecular genetics and inheritance, factors to be considered in nutritional evaluation and management (e.g., FMR1 gene function), and follow-up care.

Keywords:   fragile X syndrome, FMR1 gene function, X-linked, molecular genetics, phenotype

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