NOUN
- a genetic disease (autosomal recessive) in which an enzyme needed to metabolize galactose is deficient or absent; typically develops shortly after birth
How To Use galactosemia In A Sentence
- People who have a G6PD deficiency have the following symptoms: pale skin fatigued and tired rapid and shallow breathing abnormal/rapid heartbeat enlarged spleen yellowish tint to eyes galactosemia which is found in babies. CreationWiki - Recent changes [en]
- 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. Spy Gum | Surveillance
- In addition, the laboratory offers a specialist expertise in the diagnosis of lysosomal, galactosemia and fatty acid oxidation enzyme defects for which diseases the laboratory has a National and International reputation. Laboratory Rotation
- These conditions include sickle cell anemia, beta thalassemia, phenylketonuria PKU, hypothyroidism,8 and galactosemia. Pregnancy, Childbirth, and the Newborn
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- However, the rarity of galactosemia is a serious issue. Galactosemia: the Other Lactose Problem
- Some disorders, such as galactosemia, are initially screened on a blood spot with subsequent confirmation in red blood cells or plasma using quantitative techniques. Metabolic Disease Lab
- The classical form of galactosemia is characterized by vomiting, diarrhea, jaundice and failure to thrive within a few days after birth.
- Email: galactosemia. ureach.com www. galactosemia.com Resources for Families
- Infants with galactosemia should not be breastfed, but should receive a non – lactose - containing formula.