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Goldberg syndrome: A rare lysosomal storage disorder characterized by an enzyme deficiency (neuraminidase and beta-galactosidase) which results in a build-up of glycoproteins in the urine. There are three main subtypes: infantile, juvenile and adult forms. The early infantile form is the most severe and often results in death during infancy. More detailed information about the symptoms, causes, and treatments of Goldberg syndrome is available below.
See full list of 35 symptoms of Goldberg syndrome
Read more about complications of Goldberg syndrome.
Read more about causes of Goldberg syndrome.
Read more about symptoms of Goldberg syndrome
Medical research articles related to Goldberg syndrome include:
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Types of Goldberg syndrome
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Goldberg syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Goldberg syndrome, or a subtype of Goldberg syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Goldberg syndrome as a "rare disease".
Source - Orphanet
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