Further observations in a case of uridine diphosphate galactose‐4‐epimerase deficiency with a severe clinical presentation
- 7 May 1982
- journal article
- case report
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 6 (1), 17-20
- https://doi.org/10.1007/bf02391187
Abstract
The red-cell concentrations of galactose-1-phosphate and uridine diphosphate galactose have been studied in relation to dietary galactose in a case of uridine diphosphate galactose-4-epimerase deficiency (McK usick 23035). Uridine diphosphate galactose accumulates rapidly in response to very small amounts of galactose but the concentration of galactose-1-phosphate increases proportionately to galactose intake. The significance of the observation is discussed with respect to the pathogenesis and treatment of the disease.Keywords
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