Our Son's Rare Genetic Disorder - Syngap1

Our Son's Rare Genetic Disorder - Syngap1

Our son has an extremely rare genetic disorder….. but nothing can stop him

Dr. Tommy Martin

Toronto family tries to raise $3M to treat son's rare genetic disorder

CBC News: The National

What is SYNGAP1 | Rare Genetic Disorder | Special Needs Day in the Life | Diagnosis after 14 years

Learning our son had a rare genetic disease: It was a whirlwind.

Courageous Parents Network

Family raising awareness to rare genetic disorder after daughter diagnosed

SynGAP Research Fund - SRF - SYNGAP1 🧬 🧠

What Are SYNGAP Mutations?

Rare Disease Report

Rare Disease Day 2022 - SYNGAP1

SynGAP Research Fund - SRF - SYNGAP1 🧬 🧠

What is SYNGAP1?

SYNGAP1 Foundation

SRF Founders -- Ashley Evans & Mike Graglia - Introduction, March 2019

SynGAP Research Fund - SRF - SYNGAP1 🧬 🧠

What it’s like living with 1 working SYNGAP1 Gene!

SYNGAP1 Foundation

The Hall Family SYNGAP1 Story

SYNGAP1 Foundation

Manteca family's twin daughters live with rare genetic disorder

CBS News Sacramento

Foundations Of Rare Syngap1

Disorder Rare Disease Films

SRF | Rare Disease Day 2023 Warriors

SynGAP Research Fund - SRF - SYNGAP1 🧬 🧠

Why we need to keep talking about SYNGAP1 #S10e91

SynGAP Research Fund - SRF - SYNGAP1 🧬 🧠

Indiana 2-Year-Old One of 10 Children Ever Documented with Genetic Disorder

Celebrating Caren - Full Movie - A SYNGAP1 diagnosis 64 years in the making.

SynGAP Research Fund - SRF - SYNGAP1 🧬 🧠

SynGAP Research Fund - Heather Mefford - From gene discovery to therapy - #SYNGAP1 #SRFWebinar

SynGAP Research Fund - SRF - SYNGAP1 🧬 🧠

Improving the assessment of SYNGAP1 and related genetic conditions 🧬 | Dr Thomas Frazier

SynGAP Research Fund - SRF - SYNGAP1 🧬 🧠