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we use cookies on our website. are you happy to continue? cookie information on 26 may 2011, the rules about cookies on websites changed. this site uses cookies. some of the cookies we use are essential for parts of the site to operate and have already been set. we also use a google analytics script which uses cookies. you may delete and block all cookies from this site, but parts of the site will not work. if you continue without changing your settings, we'll assume that you are happy to receive all cookies on this website. however, you may block cookies from this site at any time from within your browser. are you happy to continue? promoting research, diagnosis, prognosis, and management of 22q11.2ds & related disorders home knowledge 22q11.2ds quick facts nomenclature guidelines reviews research commentaries thesis vault family corner about us the society officials advisors website editor the angelo digeorge medal junior investigator award the unsung hero award special service award meetings whistler 2018 programs invited speakers for professional meeting invited speakers for day 1 of family meeting invited speakers for day 2 of family meeting whistler 2018 photos previous meeting programs news news join us links connecting with colleagues comprehensive 22q centres 22q clinics around the world family support organizations other societies contact us a | a -- -- the who we are: we are a group of researchers and physicians who specialize in conditions related to the deletion and/or duplication in the chromosomal region 22q11.2 and their underlying biology. mission: to promote both basic science and clinical interdisciplinary research into the biology of the 22q11.2 region, and the diagnosis, prognosis and management of related disorders. a subsidiary goal will be to exploit the knowledge so gained for the benefit of populations of individuals with more common conditions. read more vision: to be the international leader in promoting research related to the chromosome 22q11.2 region. -- guidelines visit the guidelines section for families family corner the international 22q11.2 foundation inc. join the society structure the is a charitable incorporated organisation registered with the charity commission for england and wales. www.charitycommission.gov.uk if you wish to be involved in the administration of the or would like details of the constitution/governing document please contact us . officials chairman pete scambler (trustee) deputy chair sixto garcia-minaur (trustee) treasurer ann swillen (trustee) secretary donna mcdonald-mcginn (trustee) damian heine suñer (trustee) anne bassett (trustee) advisors bernice morrow bruno marino nicole philip jacob vorstman website editor joanne loo forthcoming events -- latest news uk parliament reviews 22q11.2ds newborn screening on june 5 th , 2018, david duguid mp raised a bill ( video link ) in the parliament of the united kingdom (uk) to require the health secretary to conduct a review into 22q11.2 deletion syndrome. it will require the national health service (nhs) to publish a strategy to deal with the condition. specifically, mr duguid called for neonatal blood spot screening to identify patients with a chromosome 22q11.2 deletion in the newborn period. on march 20 th , 2019 this initiative took a great step forward in the british parliament. please see the exchange in this video (starting from 47:36)]. david duguid mp, along with the all-party parliamentary group (appg) that he chairs, called for 22q11.2 deletion syndrome to be added to the newborn blood spot test. the prime minister, teresa may, offered to ask the department of health and social care to respond. for more information and updates, please follow david duguid on twitter or visit max appeal's website on the appg . the thanks the charity max appeal, mr. duguid, the appg, and mrs. may, for helping to add this important condition to the newborn screen test in the uk. updating: list of clinics around the world the 22q society is updating our list of 22q clinics around the world . we will be emailing you to see if you have any new information. please also feel free to contact us . thank you. 2019 'faces of 22q' calendar the 2019 'faces of 22q' calendar is now available for pre-order from the international 22q11.2 foundation . this calendar makes a lovely holiday gift to those who help individuals with 22q along this journey. by purchasing a calendar today, you will help raise much needed awareness for the 22q11.2 deletion and duplication syndromes. all proceeds benefit the international 22q11.2 foundation, inc. thank you for your support! special issue on 22q11.2 in the american journal of medical genetics just in time for 22q awareness month, the american journal of medical genetics published a special issue on 22q11.2 on october 31 st , 2018. conference photos now available photos from the conference are now available . please enjoy. if you would like to add your photos to the collection on the website of the 22q society, please contact the website editor (website_editor(at)22qsociety.org). she will provide you with the link to which photos should be uploaded. thank you. invitation to contribute to the website as the website editor mentioned at the conference, we are looking for more: - translations of existing reviews and guidelines - research commentaries - graduate theses please send your contributions to: website_editor(at)22qsociety.org thank you! 11th biennial international 22q11.2 conference completed our most recent conference in whistler, canada, has come to a conclusion. participants enjoyed great presentations and discussions in the three parts of the conference: the international brain and behaviour consortium (ibbc) meeting , the professional meeting , and the family meeting . we would like to congratulate the recipients of the angelo digeorge medal , the junior investigator award , the unsung hero award , and the inaugural special service award . photos from the conference are now available . we would also like to thank all the organizers and participants, as well as the staff at the the four seasons resort and residences whistler and the westin resort and spa whistler for this productive conference. the next conference will take place in croatia in the summer of 2020 . we hope to see you there. lisanne vervoort and tracy heung receive the junior investigator award congratulations to lisanne vervoort and tracy heung, the two recipients of the junior investigator award 2018! they received it at the international 22q11.2 ds biennial conference in whistler, canada, on july 13 th , 2018. the dempster family foundation canada receives the unsung hero award congratulations to the dempster family foundation canada , who received the unsung hero award on july 13 th , 2018, at the 11 th biennial international 22q11.2 conference in whistler, bc. profs. beverly emanuel and donna mcdonald-mcginn receive special service award congratulations to profs. beverly emanuel and donna mcdonald-mcginn , along with colleagues at the 22q and you center at the children's hospital in philadelphia (chop) and the perelman school of medicine of the university of pennsylvania, who received the inaugural special service award on july 12 th , 2018, at the 11 th biennial international 22q11.2 conference in whistler, bc. prof. bernice morrow receives the digeorge medal congratulations to prof. bernice morrow , who was awarded the angelo digeorge medal on july 11 th , 2018, at the 11 th biennial international 22q11.2 conference in whistler, bc. raising a bill in parliament to require the health secretary to conduct a review into 22q11.2ds on june 5 th , 2018, david duguid mp raised a bill ( video link ) in the parliament of the united kingdom (uk) to require the health secretary to conduct a review into 22q11.2ds. it will require the national health service (nhs) to publish a strategy to deal with the condition. specifically, mr duguid called for neonatal bloo

URL analysis for 22qsociety.org

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charitycommission.gov.uk
apps.charitycommission.gov.uk

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