What is Fabry Disease?

In this exclusive interview with Rare Disease Report, Jack Johnson of FSIG (Fabry Support & Information Group) provides a quick summary of this rare lysosomal disease.

Fabry disease is an X-linked lysosomal storage disorder that leads to excessive deposition of globotriaosylceramide ( GL-3) throughout the body. Skin, eye, kidney, heart, brain, and peripheral nervous system are highly vulnerable.

For more information about Fabry disease, visit
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