Structured Dietary Management Dramatically Improves Marked Transaminitis, Metabolic and Clinical Profiles in Glycogen Storage Disease Type IXa

Glycogen storage disease type IXa (GSD IXa) presents in childhood with hepatomegaly, poor growth, and ketotic hypoglycemia. Clinical course is usually mild, often not requiring treatment with attenuation of symptoms with increasing age. The phenotypic spectrum has recently expanded to include more s...

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Bibliographic Details
Main Authors: Indrajit S. Karande DCH, FRACP, Emily Boulter FRACP, Leah Queit APD, Shanti Balasubramaniam FRACP
Format: Article
Language:English
Published: SciELO 2016-12-01
Series:Journal of Inborn Errors of Metabolism and Screening
Online Access:https://doi.org/10.1177/2326409816682766

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