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Klinefelter Syndrome -
Beginning of paper
Klinefelter syndrome, also called testicular dysgenesis, is the phenotype of the 47,XXY genotype and is characterized by male hypogonadism and infertility. Klinefelter Syndrome is probably the most common chromosomal variation found in humans. In random surveys, it is found to appear about once in every 500 to one in every 1,000 live bor .... Middle of paper
.... have one X chromosome and one Y chromosome, but sometimes a variation will result in a male with an extra X. This is Klinefelter Syndrome and is often written as 47,XXY. There are other, less common variations such as 48,XXYY; 48,XXXY; 49,XXXXY; and XY/XXY mosaic. All of these are considered Klinefelter Syndrome variants.
The major effect of the extra X chromosome in boys with Klinefelter Syndrome seems to be the function of the testes. The t ....
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Number of words: 930
Number of pages: 4 (approx. 250 words per double-spaced page)
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