Klinefelter syndrome is a genetic condition where a male child is born with an extra X chromosome, so that his sex chromosomes are XXY rather than XY; some people with Klinefelter syndrome have more than two X chromosomes. Klinefelter syndrome is the result of random error and is not a heritable disease. While many people think of the X chromosome as solely a sex chromosome, it plays a significant role in bodily functioning, impacting brain development and growth in addition to sexual functioning. Mental retardation and phenotypic abnormalities are associated with Klinefelter syndrome and are "directly related to the number of supernumerary X chromosomes (Chen, 2013). Klinefelter syndrome is a "form of primary testicular failure, with elevated gonadotropin levels due to lack of feedback inhibition by the pituitary gland" (Chen, 2013). This results in an androgen deficiency that causes many of the symptoms associated with Klinefelter's syndrome. Other hormone levels are impacted, as well, with a typical patient with Klinefelter distributing low serum testosterone levels, and high luteinizing and FSH hormone levels (Chen, 2013). The signs symptoms associated with Klinefelter's syndrome...
In babies the symptoms include: weak muscles, slow motor development, speech delays, and docility. In boys and teenagers the symptoms include: unusual height, different body proportions than most boys, delayed or absent puberty, small or firm testicles, small penis, enlarged breast tissue, low energy levels, shyness, learning problems, and weak bones. In men, additional signs and symptoms include: infertility, decreased facial and body hair, and a decreased sex drive (Mayo Clinic Staff, 2013).Our semester plans gives you unlimited, unrestricted access to our entire library of resources —writing tools, guides, example essays, tutorials, class notes, and more.
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