GAUCHER DISEASE, QUANTITATIVE, BLOOD

Gaucher disease is an autosomal recessive lysosomal storage disease that leads to accumulation of glucocerebroside in tissues. Type 1 Gaucher disease is the commonest & is Non Neuronopathic whereas Types 2 & 3 are Neuronopathic. Types 1 & 3 Gaucher disease can be easily treated by enzyme replacement therapy.

  • Test Type:
  • Pre-test Information:
    Clinical details must accompany sample.
  • Report Delivery:
    Sample Daily by 4 pm; Report 4 Days
  • Components:
    0

Sample Report