FoxP1 Syndrome Awareness Day March 13 With image of a Fox wearing round glasses

March 13 was chosen as FOXP1 Syndrome Awareness Day because the FOXP1 gene is located on chromosome 3p13
#FoxP1

Image of a Zebra Show your stripes on rare disease day 28th February

Fox Facts The FoxP1 gene acts like a boss that tells many other genes what to do while the brain is developing FoxP1 Foundation

I support rare disease day 28 February 2026 FoxP1 Foundation

Raising awareness of FoxP1 Syndrome on Rare Disease Day 28th February 2026

#FoxP1 #ShowYourStripes

I have 11, mostly in window seat, and now I have fox cushion envy. ❤️ 🦊

#FoxP1

Enjoyed my time at the @foxp1foundation.bsky.social meeting in the Netherlands. So great to see lots of exciting #FOXP1 related research and meet so many inspiring parents 🦊🧪

Karl Whitney opens the IFF conference.

The International FOXP1 Foundation 2025 Family conference has started. Thanks Karl Whitney for the opening address. “The IFF provides hope, hope to help families to thrive with increase involve in the community”. #FOXP1, #Community #Support

Cell-type-specific roles of FOXP1 in the excitatory neuronal lineage during early neocortical murine development Ortiz et al. leverage mice with loss of FOXP1 in their cortical progenitors. Detailed cell-type-specific genomic and epigenetic alterations are described, with key findings in progenitors related to a...

Fab new study on #FOXP1 and its role during cortical development from Gena Konopka and her team 🧪🧠🦊👏

International FoxP1 Foundation fox graphic Rare disease day 28 February 2025

Zebra graphic Show your stripes on rare disease day February 28th #ShowYourStripes

🦊 #FoxP1
🦊 #RareDiseaseDay
🦊 #ShowYourStripes

Multi coloured banner with the words I support Rare Disease Day 29th February 2024

FOXP1 foundation poster - What is FOXP1 syndrome? FOXP1 syndrome is a rare disease caused by a change on the FOXP1 gene located on chromosome 3

Sharing in support of
Rare Disease Day 2024

#ShowYourColours #ShowYourStripes
#FoxP1

🧬 🧬 🧬 🧬

#FOXP1
Las familias, cuando reciben un diagnóstico de una enfermedad rara, no se curan inmediatamente, pero descansan. Ya saben que "lo suyo" tiene un nombre. También es muy importante ponerse en contacto con similares. Ojalá llegue pronto ese mensaje de apoyo. https://t.co/afkOsaumr9