What is SYNGAP1?
SYNGAP1 is a rare genetic disorder that affects brain development, leading to seizures, developmental delays, and intellectual disabilities.
Health / Rare Diseases
CNBC's Becky Quick is publicly sharing her family's journey with her daughter Kaylie's rare genetic disorder, SYNGAP1, and launching CNBC Cures to advocate for rare disease awareness.
Becky Quick's decision to share her daughter's story highlights the challenges faced by families dealing with rare diseases. SYNGAP1, a genetic disorder with no known cure, requires significant care and resources. The CNBC Cures initiative aims to bring together researchers, investors, and patients to accelerate the development of treatments and improve the quality of life for those affected. Quick's public platform provides a powerful voice for this often-overlooked community.
*Actionable Takeaway:* Understanding and awareness are the first steps toward supporting families affected by rare diseases. Learn more about SYNGAP1 and CNBC Cures to contribute to the cause.
SYNGAP1 is a rare genetic disorder that affects brain development, leading to seizures, developmental delays, and intellectual disabilities.
CNBC Cures is an initiative launched by CNBC to raise awareness and support for the 30 million Americans living with rare diseases.
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