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There are three major types of Down Syndrome. The child is most likely to have Trisomy 21, meaning presence of extra genetic material on the 21st pair of chromosomes resulting from an anomaly in cell division during development of the egg or sperm or during fertilization. 95% of people with DS have Trisomy 21. Around 4% have Translocation, where the extra chromosome 21 broke off and became attached to another chromosome. About 1% of those affected with DS have Mosaicism, where only some cells have Trisomy 21.The extra genes cause the characteristics that we know as Down syndrome. They also receive all other traits from there parents thus causing a combination of features typical of Down syndrome on top of the individual features from their parents...
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