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Klinefelter Syndrome
A genetic condition in males characterized by the presence of an extra X chromosome, leading to symptoms like reduced muscle mass, facial hair, and infertility.
Fragile X Syndrome
A genetic disorder caused by a mutation on the X chromosome, leading to developmental problems including learning disabilities and cognitive impairment.
Down Syndrome
A hereditary condition resulting from a partial or complete extra third chromosome 21, leading to intellectual and developmental delays.
XYY Syndrome
A genetic condition in males characterized by an extra Y chromosome, which can be associated with tall stature, learning difficulties, and other symptoms.
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