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These medical condition or symptom topics may be relevant to medical information for Type 2 infantile Gaucher disease:
Type 2 infantile Gaucher disease: Type 2 infantile Gaucher disease is listed as a type of (or associated with) the following medical conditions in our database:
Gaucher Disease (medical condition): 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.
Gaucher Disease: Gaucher (pronounced "go-SHAY") disease is an inherited illness caused by a gene mutation. (Source: Genes and Disease by the National Center for Biotechnology)
Gaucherís disease is an inherited metabolic disorder in which harmful quantities of a fatty substance called glucocerebroside ... (Source: excerpt from NINDS Gaucher's Disease Information Page: NINDS)
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