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Fabry disease, from early signs to critical symptoms

Fabry is a rare genetic disease caused by a variant, or mutation, in the GLA gene. The gene provides the plan for an enzyme called alpha galactosidase (alpha-Gal A).  Read more >

Fabry disease in women: genetics and disease progression

Did you know that women with Fabry, on average, get diagnosed with Fabry 10 years after first experiencing symptoms?  Read more >

Fabry disease: disease overview and personalized support for you and your family

Fabry is a rare genetic disease caused by a genetic variant, or mutation, in the GLA gene.  Read more >

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