DiGeorge syndrome

DiGeorge syndrome (22q11.2 deletion syndrome, or 22q11.2DS) is best managed in a multispecialty framework.[16]Boot E, Óskarsdóttir S, Loo JCY, et al. Updated clinical practice recommendations for managing adults with 22q11.2 deletion syndrome. Genet Med. 2023 Mar;25(3):100344. https://www.gimjournal.org/article/S1098-3600(22)01028-0/fulltext http://www.ncbi.nlm.nih.gov/pubmed/36729052?tool=bestpractice.com ​[52]Óskarsdóttir S, Boot E, Crowley TB, et al. Updated clinical practice recommendations for managing children with 22q11.2 deletion syndrome. Genet Med. 2023 Mar;25(3):100338. https://www.gimjournal.org/article/S1098-3600(22)01018-8/fulltext http://www.ncbi.nlm.nih.gov/pubmed/36729053?tool=bestpractice.com ​ Because different features of the disorder are characteristic at different life stages, frequent and long-term follow-up by a single centre or provider is beneficial. The specific testing and intervention required at a given visit also depend on the specific manifestations of the disorder in a specific patient. Awareness of the common complications will help the provider to anticipate potential problems and identify them early.