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47,XXY (Klinefelter Syndrome)

ID: si55552301
47,XXY, also known as Klinefelter Syndrome, is a congenital male chromosomal abnormality which occurs in approximately one in every five hundred male births, resulting in an XXY configuration rather than the typical XY. This illustration describes the symptoms and how the effects of the genetic mutation can be managed and how males diagnosed with the syndrome can thrive.

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