Fabry's Disease Index

Featured: Fabry Disease Main Article
Fabry disease (Fabry's disease, alpha-galactosidase-A) is a genetic disorder with symptoms such as burning sensations in the hands, small-raised reddish-purplish blemishes on the skin, fever, decreases sweating, and GI difficulties. Fabry disease patients are at increased risk of heart attack, heart disease, kidney failure, and stroke. Symptoms of Fabry disease can be treated with medication.

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Fabry Disease Glossary

Terms related to Fabry's Disease:

Alpha-galactosidase Deficiency

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