
Foxg1 Research Foundation
FOXG1 syndrome is a childhood neurological genetic disorder and is a key to understanding many brain disorders. We are pioneering research to find a cure. The FOXG1 Research Foundation is the global organization dedicated to a cure for FOXG1 syndrome. The FOXG1 Research Foundation (FRF) is dedicated to accelerating research to find a cure for every child (and adult) in the world with FOXG1 syndrome, a severe neurological, typically non-hereditary, genetic disorder. Scientists believe The research for FOXG1 can help solve brain disorders affecting millions, such as autism, Alzheimer's, brain cancer and more. The FRF is determined to save lives and give so many the able life they deserve.

Founded
2018
4100
X (Twitter)
865
Address
Sands Point
FOXG1 Research Foundation FOXG1 RESEARCH FOUNDATION DEDICATED TO CURE FOXG1 SYNDROME The FOXG1 Research Foundation FRF is the parentled global organization driving the research to cure FOXG1 syndrome and related neurological disorders while supporting and advocating for patients and families. Science Patients Community What is FOXG1 Syndrome. FOXG1 syndrome is a rare neurological genetic disorder that greatly impacts brain development and typically causes epilepsy and physical and cognitive disabilities. Most children with FOXG1 syndrome cannot walk or talk or take care of their basic needs.
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