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Klinefelter syndrome
Klinefelter syndrome is genetic or not? Mean it can transfer from father to baby or not?. Reason behind this?
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Klinefelter syndrome (KS) also known as 47,XXY or XXY, is the set of symptoms that result from two or more X chromosomes in males.[2] The primary features are sterility and small testicles.[2][8] Often, symptoms may be subtle and many people do not realize they are affected.[1] Sometimes, symptoms are more prominent and may include weaker muscles, greater height, poor coordination, less body hair, breast growth, and less interest in sex.[1] Often it is only at puberty that these symptoms are noticed.[4]Intelligence is usually normal; however, reading difficulties and problems with speech are more common.[1] Symptoms are typically more severe if three or more X chromosomes are present Klinefelter syndrome usually occurs randomly.[3] An older mother may have a slightly increased risk of a child with KS.[3] The condition is not typically inherited from one's parents.[3] The underlying mechanisms involves at least one extra X chromosome in addition to a Y chromosome such that the total chromosome number is 47 or more rather than the usual 46.[9] KS is diagnosed by the genetic test known as a karyotype.[4]    Are U married? Whats app me Nine Five Nine Five Seven Three Zero Triple Five
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Symptoms of klinefelter syndrome
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Disclaimer : The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding your medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website.