Trisomy 21

From The School of Biomedical Sciences Wiki
Revision as of 20:08, 28 November 2017 by 170067861 (talk | contribs) (added links)
Jump to navigation Jump to search
The printable version is no longer supported and may have rendering errors. Please update your browser bookmarks and please use the default browser print function instead.

Trisomy 21 is the name given to the non-disjunction  of homologous pairs of chromosomes 21 which leads to Down syndrome. "Trisomy" because, due to a nondisjunction event (failed separation of the chromosome pairs to separate during stage 1 or 2 of meiosis), there is an extra copy of chromosome 21 in one of the gametes. At fertilisation, this gamete will cause the zygote to contain 3 copies of the chromosome 21.