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Similar content being viewed by others Introduction Fabry disease is a rare X-linked inherited disorder that causes defects in the glycosphingolipid metabolic pathway that result from the deficient or absent activity of the lysosomal enzyme -galactosidase A (-Gal A) 1

More serious side effects are rare but can include allergic reactions

The patients suitability is a key factor as is the expertise of the professional performing the treatments

General best practices include: Store under recommended refrigerated conditions where applicable Protect from direct sunlight Keep the vial tightly sealed Avoid contamination Discard if the solution becomes cloudy or contains visible particles Analytical Quality Matters As with all laboratory consumables, quality and traceability are important

doi: 10.1210/mend29871 213 OrthDN

Arch Oral Biol 1975