
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.
825300929
EIN
2018
Founded
Sands Point, NY 11050-1903 USA
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foxg1research.org
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Foxg1Research
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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.
Neurology, Neuroscience Brain Disorders
23 Vacancy
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