galactose epimerase造句

• The differential diagnosis for elevated galactose concentrations in blood on a newborn screening result can include other disorders of galactose metabolism, including galactokinase deficiency and galactose epimerase deficiency.
• On initial screening, which often involves measuring the concentration of galactose in blood, classic galactosemia may be indistinguishable from other inborn errors of galactose metabolism, including galactokinase deficiency and galactose epimerase deficiency.
• Galactose epimerase deficiency is an autosomal recessive disorder, which means the defective gene is located on an autosome, and two copies of the defective gene-one from each parent-are required to inherit the disorder.