Congenital Adrenal Hyperplasia
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Take Control of PKU (Phenylketonuria)
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Biotinidase Deficiency
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Galactosemia
Galactosemia is a hereditary disease that is caused by the lack of a liver enzyme required to digest galactose. Galactose is a breakdown product of lactose , ...
www.savebabies.org/diseasedescriptions/galactosemi...
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Parents of Galactosemic Children, Inc.
Information about galctosemia and a resource for families living with galactosemia.
www.galactosemia.org/
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Your PKU Food Store:Low Protein Food
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Congenital Hypothyroidism
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Galactosemia - Wikipedia, the free encyclopedia
Nov 21, 2008 ... Galactosemia is a rare genetic metabolic disorder which affects an individual's ability to properly metabolize the sugar galactose. ...
en.wikipedia.org/wiki/Galactosemia
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Galactosemia - Genetics Home Reference
Galactosemia is a disorder that affects how the body processes a simple sugar called galactose. A small amount of galactose is present in many foods. ...
ghr.nlm.nih.gov/condition=galactosemia
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Phenylketonurics
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Congenital Hypothyroidism
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Parents of Galactosemic Children, Inc.
Parents of Galactosemic Children, Inc. (PGC) is a national, non-profit, volunteer organization whose mission is to provide information, support, ...
www.galactosemia.org/galactosemia.asp
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galactosemia: Definition from Answers.com
More about Galactosemia: Causes and symptoms Diagnosis Treatment Prognosis Prevention Resources Galactosemia Definition Galactosemia is an inherited
www.answers.com/topic/galactosemia
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Galactoses
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MedlinePlus Medical Encyclopedia: Galactosemia
Oct 20, 2008 ... The alternate names, a summary and list of major features of galactocerebrosidase deficiency.
www.nlm.nih.gov/medlineplus/ency/article/000366.ht...
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GANES
My name is Angie Forsyth, and I am the founder and current president of GANES - the Galactosemia Association of the North Eastern States. ...
www.galactosemia.com/
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Galactosemia
Galactosemia is an inherited disorder characterized by an inability of the body to utilize galactose. Galactosemia means "galactose in the blood ". ...
depts.washington.edu/transmet/gal.html
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Newborn Screening Program - Galactosemia
Galactosemia is an inherited defect of galactose metabolism caused by an enzyme ... Although infants with galactosemia may appear normal at birth, within a few days ...
www.idph.state.il.us/HealthWellness/fs/galactosemi...
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Inflammatory Bowel Disease
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