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Was (wer) ist karyotype$42097$ - definition
![The [[cell cycle]].](https://commons.wikimedia.org/wiki/Special:FilePath/Animal cell cycle-en.svg?width=200 "The [[cell cycle]].")
![Chromosomes at various stages of [[mitosis]]. Karyograms are generally made by chromosomes in prometaphase or metaphase. During these phases, the two copies of each chromosome (connected at the [[centromere]]) will look as one unless the image resolution is high enough to distinguish the two.](https://commons.wikimedia.org/wiki/Special:FilePath/Condensation and resolution of human sister chromatids in early mitosis.svg?width=200 "Chromosomes at various stages of [[mitosis]]. Karyograms are generally made by chromosomes in prometaphase or metaphase. During these phases, the two copies of each chromosome (connected at the [[centromere]]) will look as one unless the image resolution is high enough to distinguish the two.")
![[[Schematic]] karyogram demonstrating the basic knowledge needed to read a karyotype.](https://commons.wikimedia.org/wiki/Special:FilePath/How to read a Karyotype.png?width=200 "[[Schematic]] karyogram demonstrating the basic knowledge needed to read a karyotype.")
.jpg?width=200 "publisher=Oxford University Press}} Revised August 2004, January 2008</ref>")
![FISH]].](https://commons.wikimedia.org/wiki/Special:FilePath/PLoSBiol3.5.Fig7ChromosomesAluFish.jpg?width=200 "FISH]].")
Wikipedia
XYY syndrome, also known as Jacobs syndrome, is an aneuploid genetic condition in which a male has an extra Y chromosome. There are usually few symptoms. These may include being taller than average, acne, and an increased risk of learning disabilities. The person is generally otherwise normal, including typical rates of fertility.
The condition is generally not inherited but rather occurs as a result of a random event during sperm development. Diagnosis is by a chromosomal analysis, but most of those affected are not diagnosed within their lifetime. There are 47 chromosomes, instead of the usual 46, giving a 47,XYY karyotype.
Treatment may include speech therapy or extra help with schoolwork, however outcomes are generally positive. The condition occurs in about 1 in 1,000 male births. Many people with the condition are unaware that they have it. The condition was first described in 1961.
