NR2F1 Foundation is excited to announce that we have voted in five new members to our board of directors! This will increase the number of board members from six up...
Posted by | May 9, 2022
The 2022 NR2F1 Family and Scientific Conference was held this year in Orlando, FL, on April 6 – 8. It was attended in-person and virtually by families from around the...
Posted by | April 8, 2022
The NR2F1 Foundation has joined the Rare Epilepsy Network, a collaborative effort of rare epilepsies. Because over 50% of individuals with BBSOAS are also diagnosed with epilepsy, being part of...
Posted by | November 18, 2021
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Posted by | November 18, 2021
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Posted by | November 18, 2021
Click the image to watch the video. Meet Zeb from the Netherlands, a young man who lives with a very rare NR2F1 disease caused by a NR2F1 gene variant, Bosch-Boonstra-Schaaf...
Posted by | November 18, 2021
October marked the first BBSOAS collaborative research meeting with Michele Studer (France), Patrick Yu Wai Man (England), Danielle Bosch and Ninke Boonstra (Netherlands), Veeral Shah, Jane Edmond, Nilesh Desai, Sophia...
Posted by | November 18, 2021
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Posted by | November 18, 2021
Mom, Cecilia shares with us all about Simon. Cuantos años tiene Simón, y cómo escogieron su nombre? How old is Simón and how did you choose his name? Simón tiene 4 años...
Posted by | November 18, 2021
Mom Ashlee shares with us all about Emma. How did you choose the name Emma? Her first name was chosen before we even started the process to have her. Emma...
