Kline-felter syndrome: Difference between revisions
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Created page with "<u> Kliene-felter Syndrome</u> <u></u> <u></u> Kline-felter syndrome is a genetic disorder found in males adding an extra X chromosme to the normal male karyotype. These in..." |
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Kline-felter syndrome is a genetic disorder found in males adding an extra X chromosme to the normal male karyotype. These individuals are usuallly refered to as 47,XXY males. | |||
This karyotype is usually present in only 1:500 to 1:1000 live births but is the most common sex chromosome aneuploidy in males. The phenotype of the disorder is usually only presented after maturation. | |||
The most common symptoms of Kliene-felter syndrome are sterility, hypergonadism, mild mental impairment and enlargment of the breasts.<ref>[(6/11/13) Kline-felter syndrome, Available at: https://en.wikipedia.org/wiki/Klinefelter_syndrome (12/11/13)]</ref><ref>[Daniel L. Hartl. (2012) Genetics: analysis of genes and genomes, 8th edition, Burlington, MA : Jones &amp; Bartlett Learning]</ref> | |||
[[Image:XXY karyotype]] | [[Image:XXY karyotype]] | ||
References | |||
<references></references> | |||
Revision as of 07:28, 16 November 2013
Kline-felter syndrome is a genetic disorder found in males adding an extra X chromosme to the normal male karyotype. These individuals are usuallly refered to as 47,XXY males.
This karyotype is usually present in only 1:500 to 1:1000 live births but is the most common sex chromosome aneuploidy in males. The phenotype of the disorder is usually only presented after maturation.
The most common symptoms of Kliene-felter syndrome are sterility, hypergonadism, mild mental impairment and enlargment of the breasts.[1][2]
References
- ↑ [(6/11/13) Kline-felter syndrome, Available at: https://en.wikipedia.org/wiki/Klinefelter_syndrome (12/11/13)]
- ↑ [Daniel L. Hartl. (2012) Genetics: analysis of genes and genomes, 8th edition, Burlington, MA : Jones & Bartlett Learning]