Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS): Features, Diagnosis and Treatment

[@michellemckeever3989]

My family was seen by Randi Hagerman. My father had fxtas, and next year, I turn 50. I'm now living in the UK near Liverpool. Where could I go to be tested ?

[@banksiasong]

Genetic testing is free on the NHS, so seeing your GP with a referral would seem the way to go.

[@bbaca101]

Is any treatment in USA for this? I have a grandson that has passed from her mom!.

[@banksiasong]

And that innocent mother inherited it from one of her parents, presumably your in-laws since you're looking for someone to blame. So your grandson has Fragile-X then. FXTAS generally affects the carriers in their 50s and 60s. Look to your local Fragile-X support group who can advise of doctors, neurologists, and educational supports.

[@bbaca101]

He passed already at age 25... doctor don't know much about here in Illinois. Was admited to a hospital and because He had no way to comunícate. Nurses they just let him starve and temor can't be controled and were very painful dead...hope one day someone find the cure.