The Ashlyn Horry Foundation is committed in providing community initiatives focusing on youth disabilities and caregivers while providing resources for development and empowerment regardless of economic status, race, religion or creed.
1p36 deletion syndrome is a genetic condition that is caused by missing part of chromosome number 1.
While individuals with this syndrome have facial features similar to their family members, they may also have the facial characteristics commonly seen in others with 1p36 deletion syndrome.
Currently, there is no specific treatment or cure for this condition. The approach to the management of children with chromosome 1p36 deletions is similar to all children who have a complicated medical condition.
- Acknowledgement - The Horry family would like to thank each of you for your prayers, thoughts, and support during this difficult time. We want to let you know that you are greatly appreciated. Please stay tuned for upcoming events as we continue to preserve Ashlyn's legacy.