Скачать или смотреть Kabuki Syndrome Foundation: Strategically Driving Research as a Community

The 2022 Kabuki Syndrome Foundation Research Conference was held virtually on November 4, 2022. This segment features Janet Lee, Executive Director and Mom to Emily who has Kabuki syndrome.

To learn more about KSF, see all research opportunities and resources, or to make a donation please visit https://www.kabukisyndromefoundation.org. Together, we can find treatments faster.

Kabuki syndrome is a rare genetic disease with no syndrome-specific treatments. The Kabuki Syndrome Foundation is dedicated to driving research efforts that show promise to treat or cure Kabuki syndrome through fundraising, knowledge-sharing, and collaborating with researchers around the world.

Join the community!
Visit https://www.kabukisyndromefoundation.org to find resources and be counted.

You can also find us on social media: @kabukisyndrome
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Thank you for supporting Kabuki syndrome research!