Chitotriosidase Role in the Monitoring and Follow-up of Treatment in Gaucher Disease: A Review
Gaucher disease (GD) is the most common lysosomal storage disorder, resulting from an inherited deficiency of the enzyme glucocerebrosidase with an accumulation of glucocerebroside within macrophages of the reticuloendothelial system. Since the introduction of enzyme replacement therapy (ERT), reproducible biomarkers h...