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Nutritional Recommendations for Patients with Glycogen Storage Disease Type II

✍ Scribed by Corrado Angelini

Book ID
117321820
Publisher
Elsevier Science
Year
2008
Tongue
English
Weight
73 KB
Volume
30
Category
Article
ISSN
0149-2918

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The infantile form of GSD II (an inherited deficiency of the lysosomal enzyme, acid Ξ± Ξ±glucosidase, Pompe disease) is a severe and invariably fatal disease characterized by a rapidly progressive generalized hypotonia, hepatomegaly, and cardiomegaly. We have recently demonstrated that African America