XXY Syndrome: What It Is, Causes, Signs and Symptoms, Diagnosis | Osmosis
osmosis.org
XXY Syndrome: What It Is, Causes, Signs and Symptoms, Diagnosis | Osmosis
XXY syndrome, also known as Klinefelter syndrome (KS), is a genetic condition characterized by the presence of an extra X chromosome (47, Learn with Osmosis
Jun 7, 2024
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Q. 3 Enlist the symptoms of Klinefelter's syndrome... | Filo
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A boy with Klinefelter syndrome (47, XXY) is born to a mother who is phenotypically normal and a father who has the X-linked skin condition called anhidrotic ectodermal dysplasia. The mother's skin is completely normal with no signs of the skin abnormality. In contrast, her son has patches of normal skin and patches of abnormal skin. (a) Which parent contributed the abnormal gamete? (b) Using the appropriate genetic terminology, describe the meiotic mistake that occurred. Be sure to indicate in
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