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https://22qfamilyfoundation.org/living-22q/22q-support-groups-links
for individuals with 22q 11.2 deletion syndrome. Our mission is to connect families and individuals affected by 22q (Velo-Cardio-Facial syndrome, DiGeorge Syndrome) and related disorders. Our son Jonah was diagnosed with 22q 11.2 deletion syndrome when he was 21 months old and is our inspiration for starting this support group.
https://www.mdjunction.com/digeorge-syndrome
The DiGeorge Syndrome Support Group is a community of patients, family members and friends dedicated to dealing with DiGeorge Syndrome, together.
https://www.mdjunction.com/forums/digeorge-syndrome-discussions/general-support/3469835-digeorge
hello,my name is meg,i live in scotland.my daughter was diagnosed yesterday with digeorge syndrome after 14years of ill health,dont know anyone else that has kids with the syndrome yet,its early days i suppose,if anyone here would like to send me some info or just want a chat then please feel free,thanks,
https://forums.studentdoctor.net/threads/some-weird-digeorge-practice-questions.1175334/
Dec 21, 2015 · Some weird DiGeorge practice questions. Thread starter Kobebucsfan; Start date Dec 21, ... DiGeorge syndrome is characterized by malformations attributed to abnormal development of the pharyngeal arches and pouches. Most commonly, the third and the fourth pharyngeal pouches are affected. ... This forum is for support and discussion only.
https://www.mumsnet.com/Talk/special_needs/512638-digeorge-syndrome
I didn't care about the DiGeorge syndrome I just wanted her well again. It was confirmed and we were told more about it. The ears, the extra digits and the quiet cry were all beginning to fit in with the symptons. It took two weeks before Amelia was well enough (although she was still on life support) for her to be able to go in for her heart op.
https://forums.thebump.com/discussion/5184144/22q11-deletion-syndrome-digeorge-vcfs
Nov 22, 2010 · 22Q11 Deletion Syndrome / DiGeorge / VCFS? thismama. July 2010 in Special Needs. Hello! I am looking for other Mama's with babies that have 22Q11 Deletion Syndrome (aka DiGeorge or Velo Cardio Facial Syndrome)? My DD will be 1 next week and I am still learning so much - would love to connect with others!
https://www.verywellhealth.com/digeorge-syndrome-overview-4584404
DiGeorge syndrome is a rare genetic disorder caused when a small part of chromosome 22 is missing. The symptoms of DiGeorge syndrome can vary both in severity and types. Some signs may be apparent at birth, such as cleft palate or a congenital heart defect, whereas others may …
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4526275/
Practical guidelines for managing adults with 22q11.2 deletion syndrome. Wai Lun Alan Fung, ... For individuals with 22q11.2 deletion syndrome ... The results of the literature search were used to guide the discussion and to support consensus recommendations with scientific evidence when possible. A relatively limited literature about this ...Cited by: 129
https://en.wikipedia.org/wiki/Velo_cardio_facial_syndrome
DiGeorge syndrome, also known as 22q11.2 deletion syndrome, is a syndrome caused by the deletion of a small segment of chromosome 22. While the symptoms can vary, they often include congenital heart problems, specific facial features, frequent infections, developmental delay, …Causes: Genetic (typically new mutation)
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