Concepedia

Publication | Open Access

Multiple Phenotypes in Phosphoglucomutase 1 Deficiency

279

Citations

21

References

2014

Year

Abstract

Phosphoglucomutase 1 deficiency, previously identified as a glycogenosis, is also a congenital disorder of glycosylation. Supplementation with galactose leads to biochemical improvement in indexes of glycosylation in cells and patients, and supplementation with complex carbohydrates stabilizes blood glucose. A new screening test has been developed but has not yet been validated. (Funded by the Netherlands Organization for Scientific Research and others.).

References

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