Think Fabry, think early treatment to help slow or prevent life-threatening disease progression.1,2
Fabry disease is classified into two main phenotypes:2,4
Classic – absent or very low α-GAL A activity, multiple-organ systems involved, presentation generally begins in childhood
Nonclassic – also referred to as late-onset, varying levels of residual α-GAL A activity and symptoms are more variable, most frequently beginning in adulthood
Considerations for initiating ERT in each of the following:3
Cardiovascular disease is the leading cause of death in Fabry disease patients.1 Undiagnosed and untreated Fabry disease leads to progressive, irreversible, life-threatening heart injury.2,3
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