Publication
Title
Natural history of three late-diagnosed classic Galactosemia patients
Author
Abstract
The authors report the natural history of three patients with late -diagnosed Classic Galactosemia (CG) (at 16, 19 and 28 years). This was due to a combination of factors: absence of neonatal screening, absence of some typical acute neonatal symptoms, and negative galactosemia screening. This report underlines the value of neonatal screening and the importance of further diagnostic testing in case of late -onset manifestations.
Language
English
Source (journal)
Molecular Genetics and Metabolism Reports
Publication
Elsevier , 2024
ISSN
2214-4269
DOI
10.1016/J.YMGMR.2024.101057
Volume/pages
38 (2024) , p. 1-5
Article Reference
101057
ISI
001170660200001
Pubmed ID
38469096
Full text (Publisher's DOI)
Full text (open access)
UAntwerpen
Faculty/Department
Research group
Publication type
Subject
Affiliation
Publications with a UAntwerp address
External links
Web of Science
Record
Identifier
Creation 29.03.2024
Last edited 05.04.2024
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