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A list of all pages that have property "AnswerDExp" with value "Galactitol accumulation is due to the deficiency or the absence of the enzyme galactose-1-phosphate uridyltransferase, which causes galactosemia. Galactosemia is an autosomal recessive disorder associated with failure to thrive, jaundice, hepatomegaly, infantile cataracts, and mental retardation.". Since there have been only a few results, also nearby values are displayed.

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    • WBR0279  + (Galactitol accumulation is due to the defi … Galactitol accumulation is due to the deficiency or the absence of the enzyme galactose-1-phosphate uridyltransferase, which causes galactosemia. Galactosemia is an autosomal recessive disorder associated with failure to thrive, jaundice, hepatomegaly, infantile cataracts, and mental retardation.fantile cataracts, and mental retardation.)
    Retrieved from "https://www.wikidoc.org/index.php/Special:SearchByProperty/:AnswerDExp/Galactitol-20accumulation-20is-20due-20to-20the-20deficiency-20or-20the-20absence-20of-20the-20enzyme-20galactose-2D1-2Dphosphate-20uridyltransferase,-20which-20causes-20galactosemia.-20Galactosemia-20is-20an-20autosomal-20recessive-20disorder-20associated-20with-20failure-20to-20thrive,-20jaundice,-20hepatomegaly,-20infantile-20cataracts,-20and-20mental-20retardation."