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Xxxy syndrome is a genetic condition characterized by a sex chromosome aneuploidy, where individuals have two extra x chromosomes Visit the focus foundation site now. [3] people in most cases have two sex chromosomes
An x and a y or two x chromosomes. 48, xxxy can result from meiotic or mitotic nondisjunction and is often considered a variant of klinefelter syndrome (47, xxy) 48,xxxy syndrome is a type of chromosome abnormality characterized by the presence of 2 extra x chromosomes in males
It is sometimes referred to as a variant of klinefelter syndrome, but differs from klinefelter syndrome in many ways and is usually more severe
Signs and symptoms of 48,xxxy syndrome can vary but may include learning difficulties 48,xxxy syndrome is a chromosomal condition in boys and men that causes intellectual disability, developmental delays, physical differences, and an inability to father biological children (infertility) Explore symptoms, inheritance, genetics of this condition. Xxxy syndrome is an abnormal chromosomal condition affects only male individuals
The name of the syndrome indicates extra sex chromosomes is the main clinical presentation of this disorder. About 48,xxxy print this page 48,xxxy syndrome, also known as xxxy syndrome, is a less common x and y chromosome condition, affecting between 1 in 17,000 and 1 in 50,000 male births 48,xxxy is caused when nondisjunction errors occur in the development of the egg or sperm, resulting in a male inheriting two extra copies of the x chromosome. A chromosomal condition in males with intellectual disability, tall stature, and infertility due to extra x chromosomes.
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