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Short "hint"

n. - A genetic disease (autosomal recessive) in which an enzyme needed to metabolize a sugar (C6H12O6) less soluble and less sweet than glucose is deficient or absent.

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Usage examples (26)
  • However, the rarity of galactosemia is a serious issue.
  • The baby can not breastfeed: The child has a birth defect or inborn errors of metabolism such as galactosemia that makes breastfeeding difficult or impossible.
  • Some disorders, such as galactosemia, are initially screened on a blood spot with subsequent confirmation in red blood cells or plasma using quantitative techniques.
  • This very rare condition is called galactosemia.
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