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.
Sample Type - Blood
Reporting Time - 4 Days
Prerequisites - No special preparation required
Price - ₹2300/-
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