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Fabry disease is a rare genetic condition. It is caused by a build-up of a particular type of fat called globotriaosylceramide (GL-3) in the body’s cells. Individuals diagnosed with Fabry disease do not produce enough of an enzyme (alpha-GAL) to break down GL-3. This fat then accumulates in cell lysosomes which eventually leads to cell damage.
For further information on the symptoms of Fabry disease visit: https://www.fabry.com.au
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