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Chromosome 22 Duplication: Family Life, Therapy, and School Support
Chromosome 22 Duplication Syndrome is a rare genetic condition caused by an extra piece of genetic material on the 22nd chromosome. Because duplications can vary in size and location, symptoms and developmental outcomes differ widely from child to child. Some children may experience delayed milestones, speech and language challenges, learning disabilities, autism-like traits, or hypotonia…
