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Galactosemia
- 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 ...
- ... 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 ...
- An infant with galactosemia is unable to use (metabolize) the simple sugar galactose, which reaches high levels in the body, causing damage to ...
- ... 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. ...
- ... such as: Cystine (cystinosis) Fructose ( fructose intolerance ) Galactose ( galactosemia ) Glycogen (glycogen storage disease) Cystinosis is the most ...
- ... of fructose intolerance are similar to those of galactosemia (inability to use the sugar galactose). Later symptoms ...
- ... trisomy 21) Ectodermal dysplasia syndrome Familial congenital cataracts Galactosemia Hallermann-Streiff syndrome Lowe syndrome Marinesco-Sjögren syndrome ...
- ... metabolism. A few of them are: Fructose intolerance Galactosemia Maple syrup urine disease (MSUD) Phenylketonuria (PKU) Newborn ...
- ... may result from other conditions, including congenital rubella , galactosemia , retrolental fibroplasia ) Persistent primary hyperplastic vitreous Retinoblastoma Toxocara ...
- ... to: Alkaptonuria Canavan disease Cystinosis Cystathioninuria Fructose intolerance Galactosemia Hartnup disease Homocystinuria Hyperammonemia Hyperparathyroidism Maple syrup urine ...