Welcome to the CAPOS blog. you are awesome! Thank you for taking five, ten minutes reading my blogs! I appreciate YOU!

CAPOS is a unique syndrome with five equally complex symptoms: CLICK HERE to find out more

About CAPOS

So, what exactly is CAPOS? A good question as old as time itself!

In essence; CAPOS syndrome is an extremely rare neurological disorder of autosomal dominant inheritance. It was first described in 1996.

In 1996, I was just starting my second semester at Simon Fraser University, I had ASL interpreters and, I’m pretty sure, access to large printed materials. However, I still had no idea why I was bumping into things or walking drunkenly. I pegged it as a vision issue; not being able to see something until it was right in front of me.

And yet, research in this weird phenomenal was gaining recognition! A few people were showing similar traits, so researchers intensified their research and determined a genetic mutation had occurred on the ATP1A3 gene, leading to defects in the following areas:

Please click each link to learn more! Don’t be shy, I know you want to learn!

Cerebellar ataxia

Areflexia

Pes cavus

Optic atrophy

Sensorineural hearing loss

there ya have it folks! CAPOS!

If you have any questions, comments or feedback, please do contact me!

Thank you!