NR2F1 Foundation

The NR2F1 Foundation is a 5 year old, 501c3 nonprofit empowering families and individuals worldwide living with rare NR2F1 gene variants through education, advocacy and research.

We are a small but mighty team of parents, volunteers and family members. The syndrome is called Bosch-Boonstra-Schaaf optic atrophy syndrome (BBSOAS) and the symptoms include intellectual disability/developmental delay, Cerebral Visual Impairment, seizures and a host of ocular impairments.

We are a cohesive, supportive and motivated team changing lives for the better every day. If you are looking to expand your resume and use your skills to make a real difference, we encourage you to apply!