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Results 1 - 10 of 11 for Galactosemia
  1. Galactosemia is a condition in which the body is unable to use ( metabolize ) the simple sugar galactose. ... Galactosemia is an inherited disorder. This means it is passed down through families. If both parents carry ...
  2. ... level of this substance causes a condition called galactosemia . ... This is a screening test for galactosemia. In normal diets, most galactose comes from the breakdown ( metabolism ) of lactose, which is found in milk and dairy products. One out ...
  3. An infant with galactosemia is unable to use (metabolize) the simple sugar galactose, which reaches high levels in the body, causing damage to ...
  4. ... based formulas should be used for infants with galactosemia , a rare condition. These formulas can also be ... free formulas: These formulas are also used for galactosemia and for children who can't digest lactose. ...
  5. ... such as: Cystine (cystinosis) Fructose ( fructose intolerance ) Galactose ( galactosemia ) Glycogen (glycogen storage disease) Cystinosis is the most ...
  6. ... of fructose intolerance are similar to those of galactosemia (inability to use the sugar galactose). Later symptoms ...
  7. ... trisomy 21) Ectodermal dysplasia syndrome Familial congenital cataracts Galactosemia Hallermann-Streiff syndrome Lowe syndrome Marinesco-Sjögren syndrome ...
  8. ... metabolism. A few of them are: Fructose intolerance Galactosemia Maple syrup urine disease (MSUD) Phenylketonuria (PKU) Newborn ...
  9. ... may result from other conditions, including congenital rubella , galactosemia , retrolental fibroplasia ) Persistent primary hyperplastic vitreous Retinoblastoma Toxocara ...
  10. ... to: Alkaptonuria Canavan disease Cystinosis Cystathioninuria Fructose intolerance Galactosemia Hartnup disease Homocystinuria Hyperammonemia Hyperparathyroidism Maple syrup urine ...
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