Gaucher disease type 3
Gaucher disease type 3: Introduction
Gaucher disease type 3: A rare inherited biochemical disorder characterized by the deficiency of the enzyme called glucocerebrosidase and accumulation of glycosylceramide (glucocerebroside). There are three forms of this disease: type 1, 2 and 3. Type 3 is a subacute neurological form which often first appears in childhood.
More detailed information about the symptoms,
causes, and treatments of Gaucher disease type 3 is available below.
Symptoms of Gaucher disease type 3
See full list of 16
symptoms of Gaucher disease type 3
Wrongly Diagnosed with Gaucher disease type 3?
Gaucher disease type 3: Related Patient Stories
Gaucher disease type 3: Deaths
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Gaucher disease type 3: Complications
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Causes of Gaucher disease type 3
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Disease Topics Related To Gaucher disease type 3
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Evidence Based Medicine Research for Gaucher disease type 3
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Research about Gaucher disease type 3
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Statistics for Gaucher disease type 3
Gaucher disease type 3: Broader Related Topics
Types of Gaucher disease type 3
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Definitions of Gaucher disease type 3:
Gaucher disease type 3 is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Gaucher disease type 3, or a subtype of Gaucher disease type 3,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Contents for Gaucher disease type 3: