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Newly diagnosed with hereditary fructose intolerance

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An 18-month-old is newly diagnosed with hereditary fructose intolerance (deficiency in Aldolase B). His mother reports he is particularly upset when he gets up in the morning or if he has not eaten in a while. Laboratory testing showed low blood glucose levels at the time of presentation. This presentation is likely due to an accumulation of fructose 1 -phosphate and inhibition of which of the pathways?

Reference no: EM132440302

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