Turner syndrome: Difference between revisions
Jump to navigation
Jump to search
No edit summary |
No edit summary |
||
| Line 1: | Line 1: | ||
Turner Syndrome is a [[Monosomic|monosomic]] condition in which only one [[X chromosome|X chromosome]] is present (XO). Instead of having a set of 44 [[Autosomes|autosomes]] + 1 pair of sex [[Chromosome|chromosomes]] (either XX or XY), the person has only 44 [[Autosomes|autosomes]] + 1 X [[Chromosome|chromosomes]]. It happens in about 1 in 5000 female births. The affected females are of a characteristic [[Phenotype|phenotype]] e.g sterile, have a short height, low hairline, small finger nails, and poor breast development with the nipples spread a distance apart <ref>Anthony JF Griffiths et al., 1990, Modern Genetic Analysis, New York : W.H.Freeman, Chapter 8</ref>. | Turner Syndrome is a [[Monosomic|monosomic]] condition in which only one [[X chromosome|X chromosome]] is present (XO). Instead of having a set of 44 [[Autosomes|autosomes]] + 1 pair of sex [[Chromosome|chromosomes]] (either XX or XY), the person has only 44 [[Autosomes|autosomes]] + 1 X [[Chromosome|chromosomes]]. Turner syndrome ocurrs as a result of nondisjunction, which is when chromosomes do not separate successfully during meiosis. It happens in about 1 in 5000 female births. The affected females are of a characteristic [[Phenotype|phenotype]] e.g sterile, have a short height, low hairline, small finger nails, and poor breast development with the nipples spread a distance apart <ref>Anthony JF Griffiths et al., 1990, Modern Genetic Analysis, New York : W.H.Freeman, Chapter 8</ref>. | ||
=== References === | === References === | ||
<references /> | <references /> | ||
<br> | <br> | ||
Revision as of 15:19, 29 November 2012
Turner Syndrome is a monosomic condition in which only one X chromosome is present (XO). Instead of having a set of 44 autosomes + 1 pair of sex chromosomes (either XX or XY), the person has only 44 autosomes + 1 X chromosomes. Turner syndrome ocurrs as a result of nondisjunction, which is when chromosomes do not separate successfully during meiosis. It happens in about 1 in 5000 female births. The affected females are of a characteristic phenotype e.g sterile, have a short height, low hairline, small finger nails, and poor breast development with the nipples spread a distance apart [1].
References
- ↑ Anthony JF Griffiths et al., 1990, Modern Genetic Analysis, New York : W.H.Freeman, Chapter 8