What is the rare SYNGAP1 genetic disease Becky Quick's daughter has?

SYNGAP1 is a genetic disorder that affects brain development, causing seizures, developmental delays, and intellectual disabilities.

What are the symptoms of SYNGAP1 disease?

Symptoms include seizures, developmental delays, intellectual disabilities, and often severe autism and apraxia.

Does Becky Quick's daughter Kaylie have autism?

Yes, Kaylie has severe autism, along with other challenges associated with the SYNGAP1 genetic disorder.

Home / Health / CNBC Anchor's Daughter Battles Rare Genetic Disease

CNBC Anchor's Daughter Battles Rare Genetic Disease

8 Jan

•

Summary

Kaylie was diagnosed with SYNGAP1, a rare genetic disorder affecting brain development.
The disease causes seizures, developmental delays, and severe autism.
Becky Quick highlights unequal access to care for families with rare conditions.

CNBC Anchor's Daughter Battles Rare Genetic Disease

Becky Quick, a co-anchor for CNBC's Squawk Box, has disclosed her daughter Kaylie's battle with SYNGAP1, a rare genetic disorder. Kaylie, now nine years old, was diagnosed with the condition before her third birthday after experiencing developmental delays and seizures discovered via an EEG.

SYNGAP1 affects the production of a key protein for brain development, resulting in intellectual disabilities, severe autism, and apraxia. Despite these challenges, Kaylie is described as a loving and determined child. Quick's essay details the emotional toll of the diagnosis and the subsequent journey of seeking therapies and medical support for her daughter.

Quick underscored the significant disparities in healthcare access, acknowledging that her public platform and resources provided advantages most families lack. She advocates for greater understanding and support for individuals with rare genetic conditions and their families.

Disclaimer: This story has been auto-aggregated and auto-summarised by a computer program. This story has not been edited or created by the Feedzop team.