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22q11.2 Deletion Syndrome: Sibling Support and Medical Advocacy Tips
DiGeorge Syndrome, also known as 22q11.2 Deletion Syndrome, is a genetic condition caused by a small missing piece of chromosome 22. While it affects each child differently, many children with 22q face a mix of challenges including congenital heart defects, immune system issues, developmental delays, feeding difficulties, and behavioral or learning differences. Families caring for…
