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Klinefelter syndrome (ks) is a chromosome variation affecting around 1 in 660 males in which an extra x chromosome is present, resulting in a genetic karyotype of 47,xxy
Karyotype analysis is required for definitive diagnosis The extra x chromosome leads to testicular hypofunction and testoste. A karyotype of 47,xxy may also be expected as mosaic with a 46,xy but the present case is rarely reported Klinefelter syndrome is a genetic disorder in which males have an additional x chromosome in their genetic code
Most males have 46 chromosomes (packages of dna) This includes one copy of an x chromosome and one copy of a y chromosome (46, xy) People with klinefelter syndrome have a total of 47 chromosomes (47, xxy). Approximately one in 1,000 boys is born with an additional x chromosome—47,xxy, the karyotype that causes klinefelter syndrome
1 this karyotype is detected at or before birth in 10 percent of.
47,xxy, commonly known as klinefelter syndrome, is a chromosomal condition that affects male development This genetic variation is characterized by the presence of an extra x chromosome in males, resulting in a 47,xxy karyotype instead of the typical 46,xy It is considered one of the most common chromosomal disorders, affecting approximately 1 in 500 to 1 in 1,000 newborn males This condition is characterized by the presence of an extra x chromosome in males, leading to the karyotype 47,xxy instead of the typical 46,xy
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