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Galactosemia
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Galactosemia
Galactosemia is a genetically inherited metabolic disorder. This disorder leaves the disabled with a partial or complete lack of the enzyme Galactose 1 Phosphate Uridyl Transferase (GALT). This enzyme is found in the bloodstream and it is used for breaking down the sugar galactose. This disorder comes in two different variations. Though there is more than one type, it is still rare, having only 1 in 80,000 births being affected by the disorder.
Classic Galactosemia is ...
Approximate word count: 677
Approximate pages: 3 (250 words per
double-spaced page) |
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