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galactosemia
(redirected from Galactosemia I)

   Also found in: Medical, Encyclopedia, Wikipedia 0.03 sec.
ga·lac·to·se·mi·a  (g-lkt-sm-)
n.
An inherited metabolic disorder characterized by the deficiency of an enzyme that is necessary for the metabolism of galactose. The disorder results in elevated levels of galactose in the blood and, if untreated, can lead to mental retardation and eye and liver abnormalities.

ga·lacto·semic adj.
ThesaurusLegend:  Synonyms Related Words Antonyms
Noun1.galactosemia - a genetic disease (autosomal recessive) in which an enzyme needed to metabolize galactose is deficient or absent; typically develops shortly after birth
inborn error of metabolism - any of a number of diseases in which an inherited defect (usually a missing or inadequate enzyme) results in an abnormality of metabolism


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Galactosemia is an inherited disorder that prevents a person from processing the sugar galactose, which is found in many foods.
Galactosemia is a rare hereditary disease leading not only to cirrhosis in infants, but, more seriously, to early, devastating illness if not diagnosed quickly.
Screening for hypothyroidism, like PKU, is now mandated throughout the US, and the test for galactosemia is required everywhere but Louisiana, Pennsylvania, and Washington state.
 
 
 
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