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Fabry Disease 

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Thrombus Formation

medical illustration of This 3D image was displayed in a pharmaceutical exhibit at a conference focused on lysosomal diseases. It features the molecule, alpha-galactosidase A, which is deficient in Fabry disease. Fabry disease is a rare genetic lysosomal storage disorder.
Next medical illustration of This diagrammatic illustration depicts the cellular and molecular pathway involved in the pathogenesis of Gaucher Disease, an inherited metabolic disorder that leads to the accumulation of  the lipid glucocerebroside in cells and certain organs. Gaucher disease causes the deficiency of an enzyme, glucocerebrosidase, that normally breaks down and recycles this lipid.

Gaucher Disease Pathway

This 3D image was displayed in a pharmaceutical exhibit at a conference focused on lysosomal diseases. It features the molecule, alpha-galactosidase A, which is deficient in Fabry disease. Fabry disease is a rare genetic lysosomal storage disorder.

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© Audra Geras