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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

  • 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® ref4-250