Hypovitaminosis D in glycogen storage disease type I

Glycogen storage disease type I (GSD I) is caused by inherited defects of the glucose 6-phosphatase complex, resulting in fasting hypoglycemia, lactic acidosis, hyperuricemia and hyperlipidemia. Sixteen out of 26 (61.5%) GSD I patients in our study had suboptimal levels (

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Bibliographic Details
Published in:Molecular genetics and metabolism 2010-04, Vol.99 (4), p.434-437
Main Authors: Banugaria, Suhrad G., Austin, Stephanie L., Boney, Anne, Weber, Thomas J., Kishnani, Priya S.
Format: Article
Language:English
Subjects:
25-Hydroxyvitamin-D
Adolescent
Adult
Bone mineral density
Child
Child, Preschool
Female
Glycogen storage disease type I
Glycogen Storage Disease Type I - metabolism
Humans
Hypoglycemia - complications
Male
Middle Aged
Osteopenia
Osteoporosis
Vitamin D
Vitamin D Deficiency - complications
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Description
Summary:Glycogen storage disease type I (GSD I) is caused by inherited defects of the glucose 6-phosphatase complex, resulting in fasting hypoglycemia, lactic acidosis, hyperuricemia and hyperlipidemia. Sixteen out of 26 (61.5%) GSD I patients in our study had suboptimal levels (
ISSN:1096-7192
1096-7206
DOI:10.1016/j.ymgme.2009.12.012