SYNGAP1 research at the Patrick Wild Centre

Arulmurugan Kalyanasundaram is raising money for The University of Edinburgh

Team: Hope for Syngap

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500 miles

A SYNGAP1 gene mutation can cause a variety of symptoms that can range from mild to severe. The most common symptoms include learning difficulties, epilepsy, behavioural challenges, autism, and sensory processing disorder. Research is vital.

Story

A SYNGAP1 gene mutation can cause a variety of symptoms that can range from mild to severe. The most common symptoms include learning difficulties, epilepsy, behavioural challenges, autism, and sensory processing disorder. Research is vital.

I am fundraising with my friends to raise awareness of this rare condition.

Our team plans to do 3600KM by walk, run, swim, cycle by Oct 2024 and I hope to do 800KM of those..

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£10.00
+ £2.50 Gift Aid
Online
£10.00
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£0.00

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