What is the treatment for Fabry disease?

There is currently no cure for Fabry disease. Despite this, enzyme replacement therapy (ERT) can help manage some of its symptoms by replacing the alpha‐GAL enzyme that is deficient. The replacement enzyme is usually given fortnightly to the patient via intravenous (IV) infusion to help break down the particular type of fat called globotriaosylceramide (GL-3) that has built up in the cells. The cells and body organs can start to work properly and people can experience some symptomatic relief. Fabry disease can affect different organs of the body and those affected may have high blood pressure or irregular heartbeats. They may need heart medications to lower their blood pressure and control their heart rate. Other medications may be required depending on the symptoms present. It is important to discuss treatment options with your doctor.

For further information on Fabry disease and treatment options visit: https://www.fabry.com.au