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Among the more common features associated with this … Standard trisomy 21- Individuals who have standard trisomy 21 have three copies of chromosome 21 in every cell in their body. 10q26 deletion syndrome is a condition that results from the loss (deletion) of a small piece of chromosome 10 in each cell. About 95% of … Down syndrome is caused by having three copies of chromosome 21 instead of two copies. It is usually associated with physical growth delays, mild to moderate intellectual disability, and characteristic facial features. The signs and symptoms of 10q26 deletion syndrome vary widely, even among affected members of the same family. Down syndrome or Down's syndrome, also known as trisomy 21, is a genetic disorder caused by the presence of all or part of a third copy of chromosome 21. This is denoted by the karyotype 47,XX,+21 for females and 47,XY,+21 for males. This paper describes a study of phonological skills in six children with Down syndrome who were participating in a larger study of literacy development. Down syndrome is the most common chromosome abnormality in humans, occurring in about 1 in 800 live births. Opinions vary as to whether phonological awareness is a necessary prerequisite for beginning reading, or a product of learning to read. There are three ways this extra copy of chromosome 21 can cause Down syndrome. The deletion occurs on the long (q) arm of the chromosome at a position designated 10q26. 1 Down syndrome is associated with a …