Fabry's disease

What is Fabry's disease?

Fabry disease is a rare genetic disorder that causes a lack of or decreased amount of alpha-galactosidase-A, an enzyme that is needed for the body to break down a specific type of fat. As a result, this fat can accumulate throughout the body which can lead to complications with many organs.

How do members experience Fabry's disease?

Top 5 symptoms reported by people with Fabry's disease*

*Reports may be affected by other conditions and/or medication side effects. We ask about general symptoms (anxious mood, depressed mood, fatigue, pain, and stress) regardless of condition.

Are you experiencing one or more of these symptoms? Check your symptoms and clarify your options for care using

Top treatments taken by people for Fabry's disease*

We currently don't have enough shared data that is made public for this condition.

Let's build this page together! When you share what it's like to have Fabry's disease through your profile, those stories and data appear here too.

Who has Fabry's disease on PatientsLikeMe?

Age

Age Proportion # of patients
<20 0
20s 1
30s 11
40s 19
50s 19
60s 14
70+ 3

Distribution of sex

Sex

Sex Proportion # of patients
Male 21
Female 47
Learn more about our community’s experience with Fabry's disease.

Talk to people with Fabry's disease

77

77

members say they have this condition

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Endocrine, Metabolism and Nutrition,Skin, Hair, and Nails,Neurological and Brain

Learn from others like you living with Fabry's disease.
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