Hao-Fountain Syndrome

Our latest newsletter is out! Make sure to check it out today. #usp7 #hafous #haofountainsyndrome usp7.salsalabs.org/november2024ne…

We are proud to announce the 2026 Young Investigator Draft Class! 10 Researchers. $200,000 in seed grants. Endless potential for tomorrow. Join us to celebrate: charity.pledgeit.org/YID2026

We are excited to announce our collaboration with @UpliftingAth to award Emilie Korchak a $20k grant in support of her Hao-Fountain Syndrome research! Join us in celebrating Emilie at the Young Investigator Draft on January 31! #YID26 bit.ly/yid2026

We can’t thank our researchers enough! We love you! @TTUVetMed @klementinafontacer #RareDiseaseDay2025 #haofountainsyndrome #RareDiseaseDay #usp7

Very happy to share our new collaborative paper describing a key role for USP7-PRC1.1 in neural differentiation, now in @GenesDev And congratulations to the PhD student, Axelle, on her 1st research paper. #USP7 #epigenetics #neural  @FoundationUSP7 m.genesdev.cshlp.org/content/early/…

Registration for our 2025 Hao-Fountain Syndrome Symposium and Family Conference is open. usp7.org/register #hafous #usp7 #conference

new international collaborative work incl our group on Hao-Fountain syndrome and the mechanisms underlying USP7 published in Genes & Development #raredisease #USP7 #epigenetics #drosophila #neurons @JeffreyHaren @YAtlasi, Peter Verrijzer, @druoph @FoundationUSP7 @ErasmusMC

Save the date! Our 2025 Symposium and Family Conference will be held September 18-19 in Nashville. Registration will open in February. #usp7 #hafous #symposium #familyconference

Riley’s Journey is written from her mother's perspective, chronicling the journey to Riley's diagnosis of Hao-Fountain Syndrome. Visit usp7.org/blog/rileysjou… #raredisease #usp7 #haofountainsyndrome

@YAtlasi It was wonderful to meet you! Thank you for being part of our symposium. We enjoyed your presentation and were so glad you could be there!

Had a fantastic time in Atlanta attending the USP7 symposium. Huge thanks to the @FoundationUSP7 for the invitation; it was an absolute pleasure meeting both patients’ families and the incredible researchers in the field. #USP7

We still have sponsorship opportunities available for our upcoming Hao-Fountain Syndrome Symposium and Family Conference. Sponsorships will directly contribute to the success of this event. We are offering five levels of sponsorship. Visit lnkd.in/ekZNBTqT

Attending our Symposium and Family Conference on September 24? If so, make sure to book your hotel room by tomorrow, September 2nd, to get our exclusive rate of just $209 per night! Book now to take advantage of this exceptional rate. hyatt.com/en-US/group-bo… #familyconference

Our conference is just around the corner! Make sure to register today and book your room before September 2nd to ensure you get our exclusive room rate of just $209 per night! We can't wait to see you at the Grand Hyatt Atlanta on September 24th. usp7.org/2024-symposium

One of our beautiful Hao-Fountain Syndrome Warriors, an amazing young woman from Australia is running a 10k in honor of Hao-Fountain Syndrome and raising funds for research. Show her your support by making a donation today: usp7.salsalabs.org/tanaefundraiser #usp7 #hafountainsyndrome

Just launched in our merch shop - 2024 Hao-Fountain Syndrome conference shirts and tote bag! Order today. #symposium #familyconference #usp7 #haofountainsyndrome bonfire.com/store/foundati…

Be part of something amazing! Join us for our 2024 Hao-Fountain Syndrome Symposium and Family Conference in Atlanta on September 24. Register today! usp7.salsalabs.org/2024Symposiuma… #HAFOUS #raredisease #HaoFountainSyndrome #USP7 #symposium #familyconference #atlanta

Our Lunch and Learn is on the calendar! Join us on June 17 for an amazing session all about precision medicine. Click the link to learn more and to sign up today! You won't want to miss it! usp7.salsalabs.org/lunchandlearnj… #usp7 #hafous #haofountainsyndrome #lunchandlearn

Calling all Hao-Fountain Syndrome families in the United States! Are you interested in learning more about your child's disease while also helping advance scientific research? Consider donating your child’s blood sample to an anonymous biorepository. usp7.salsalabs.org/researchopport…

Imagine. #hafous #usp7 #haofountainsyndrome #raredisease

Recently diagnosed? Sign up for our New Family Orientation and Information Zoom Session on June 2! We will record the session so if you can't attend you'll be able to watch it later, but make sure to sign up so you can receive the recording. Sign up here: usp7.salsalabs.org/newfamilyorien…