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Gaucher Disease, the most common inherited lysosomal storage disorder, is caused by glucocerebrosidase deficiency due to mutations in the GBA gene. The Gaucher Disease StripAssay® identifies the most frequent mutations and recombinant alleles.
Gaucher Disease, the most common inherited lysosomal storage disorder, is caused by glucocerebrosidase deficiency due to mutations in the GBA gene. The Gaucher Disease StripAssay® identifies the most frequent mutations and recombinant alleles.
Gaucher Disease
- Clinical symptoms include enlargement of several organs like spleen, liver, lungs, bones and brain due to glucocerebroside buildup.
- Anemia, easy bruising, bone pain and fractures may occur as associated symptoms.
- Gaucher Disease has no cure.
- Treatment options for some forms of this disease include enzyme replacement therapy.
Product Details
| Gaucher Disease StripAssay® |  | 4-250 |