Yes een megagroot artikel over #22q11ds in het AD supergoed want hoe meer informatie er bekend is hoe meer begrip er (hopelijk)komt voor mensen met dit syndroom!Dat is waar ik me voor inzet en voor in zal blijven zetten! #RT voor meer bekendheid #22q11ds !

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Very proud of the newest member of our team Julie Husmann for a great presentation on social functioning profiles in 22q11DS at the 5th European conference

#22q11ds
#RT wordt op prijs gesteld !

#22q11ds ….????

Very happy to share the new clinical recommendations for children & youth, and adults (separate link below) with 22q11DS. sciencedirect.com/science/articl… #22q #22q 11DS

🙋🏽‍♀️ Avui hem vengut fins a l'Institut Pere Mata per reunir-nos amb la resta de grups de l'Estudi pilot per a la implementació d'una eina de cribat per CNVs en pacients amb trastorn del neurodesenvolupament (22q11DS com a model), el qual s'emmarca dins la convocatòria IMPaCT. (1/5)

Here is my life story one more time its about me dealing with the daily struggle and challenges that #22q11ds brings. Despite my life is diffrent then most i try to get the best out of it and spread happyness around the world!
chilloutradio.com/professional-w…

Study of interest for teens living with 22q11DS

#22q #22q 11 #22q awareness #study

Willen jullie me opvrolijken door dit artikel waarin 22q11ds heel duidelijk word uitgelegd te retweeten voor meer bekendheid voor 22q11ds!!!❤️❤️❤️

LivinInFucktardia2 Parent Study for Chr. 11 deletion syndrome: The Internet was the main source of information and knowledge about their child’s disease for 93% of respondents. The physicians’ knowledge about 22q11DS was positively rated by 14%. ojrd.biomedcentral.com/articles/10.11…

22Q11 Stichting NL

#22q11ds

Video of me and Quinn Bradlee 10 years ago Quinn has #22q11ds and interviews people who have learning disabilitys like me

youtube.com/watch?v=47dDU9…

The next 22q11 Europe conference will take place on November 18th and 19th 2023 in Dublin. To present your more recent findings on #22q11DS , the deadline for abstract submission has been extended until July 15th! Abstracts (250 words) should be sent to [email protected]!

RTÉ news2day Molly O’Connor RAiN RARE Ireland Rare Diseases Ireland Appreciate the coverage today Molly O’Connor and RTÉ news2day for individually rare collectively common #RareDiseases - a significant cause of physical intellectual and sensory disabilities
#IamNumber17 #22q11DS

medicalxpress.com/news/2023-05-e…
people with the copy variant number 22q11.2 deletion syndrome ( #22q11DS ) probes the excitatory-inhibitory neurotransmitter system prior to the onset of #psychosis .

Must read: Updated clinical recommendations for the management of children and adults with 22q11.2 deletion syndrome. #22q 11DS #22q @booterik bit.ly/3I9UyHd bit.ly/3HSg5Tk

'.....future research can educate against the plight of 22q11DS families. It can enlighten health care professionals in buffering against associated stigma, blame, and self-doubt, and in fostering psychological well-being' #22q #FamiliesUnderSiege
psycnet.apa.org/record/2016-45…

We found this to be the case! GSK3β-related synaptic mechanisms may thus underlie the observed dysconnectivity in human 22q11DS

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