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biological

Judged: two independent readers; copy check clear.

trisomy 21

trisomy 21 Trisomy 21 is a genetic condition in which chromosome 21 is present in extra full or partial form.

Trisomy 21 is a genetic condition in which chromosome 21 is present in extra full or partial form. It is linked with a recognizable pattern of physical differences, moderate to severe intellectual disability, and higher rates of heart and digestive abnormalities, leukemia, and unusually early Alzheimer-type brain disease.