Please verify your email address to receive email notifications.

Enter your email address

We have sent you a verification email. Please check your inbox and spam folder.

Unable to send verification, please refresh and try again later.

  • Q&A with Australian Health Practitioners

    What is Fabry disease?

    answer this question

  • Find a professional to answer your question

  • Team HealthShare

    HealthShare Member

    Fabry disease is a rare genetic condition. This disease results from a build-up of a particular type of fat called globotriaosylceramide (GL-3) in the body’s cells, and a lack of an enzyme (alpha-GAL) which would ordinarily break this fat down. The build-up of these fats impairs the cells’ ability to function. Most symptoms of Fabry disease develop as a result of the accumulation of these fats in the body’s cells. The disease is progressive which means the symptoms are likely to worsen over time. 

     

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

    Reply to this post
     · 
    Report
    Reply to this post

    You must be a Health Professional to reply to this post. to your account or now (it's free).

answer this question

You must be a Health Professional to answer this question. Log in or Sign up .

Empowering Australians to make better health choices