Illustrated · 2 min
Nondisjunction
During cell division, DNA is duplicated and then divided equally into two daughter cells. This way, each new cell contains all the genetic information it needs to function.

Image source: By Mysid [Public domain], via Wikimedia Commons
Nondisjunction occurs when chromosomes fail to separate during division, causing chromosome abnormalities. This can occur in meiosis or mitosis. Here's more on nondisjunction.
During mitosis, it can occur during anaphase. This results in two diploid daughter cells. One cell will have an extra chrosmome (). This is called trisomy, which often happens with chromosome 21. The other cell will have a missing chromosome (). This is called monosomy. Nondisjunction during mitosis will be limited to one cell or one type of tissue because it originates in a somatic (non-sex) cell.

Image source: By Alex Federspiel CC BY-SA 4.0, via Wikimedia Commons
When nondisjunction occurs during meiosis, it can happen during anaphase I or anaphase II. When it occurs during anaphase I (as seen in the diagram below, on the right), the homologous chromosomes do not separate. The cells then go through meiosis II normally, resulting in four possible cells. Since this is meiosis, these cells are called gametes and are haploid. All daughter cells are affected. Two of the gametes will have an extra copy of the chromosome and the other two will not get any copies of that chromosome.

Image source: By Tweety207 CC BY-SA 3.0, via Wikimedia Commons
The bottom row of the diagram shows what the cells would look like after fertilization. Two of the cells would have an extra chromosome () and two cells have a missing chromosome (). Notice that the diagrams only include the chromosome which undergoes nondisjunction, meaning that the "empty" cells actually contain other chromosomes which did not undergo nondisjunction.
When nondisjunction occurs in meiosis II, cells divide normally during anaphase I (homologous chromosomes separate correctly), but sister chromatids fail to separate during anaphase II (as seen in the diagram above, on the left). This again results in four possible haploid gametes. Two of the gametes have the normal, single copy of the chromosome, one will have two copies of the chromosome, and one won't have any copies of the chromosome.
The bottom row shows what the cells would look like after fertilization. Here only two of the cells are affected. One cell shows trisomy () and the other shows monosomy ().

