Can a girl have Klinefelter’s syndrome?
Klinefelter syndrome (47,XXY) results from an additional X chromosome on an XY background; therefore, this condition affects only males..
How is Klinefelter’s syndrome caused?
Klinefelter syndrome is caused by an additional X chromosome. This chromosome carries extra copies of genes, which interfere with the development of the testicles and mean they produce less testosterone (male sex hormone) than usual.
Where does Klinefelter’s syndrome occur?
Klinefelter syndrome occurs as a result of a random error that causes a male to be born with an extra sex chromosome. It isn’t an inherited condition. Humans have 46 chromosomes, including two sex chromosomes that determine a person’s sex. Females have two X sex chromosomes (XX).
What is the life expectancy of Klinefelter syndrome?
According to research, Klinefelter syndrome can shorten your life expectancy up to two years. However, you can still live a long, full life with this condition. The earlier you get treatment, the better your outlook will be.
CAN XXY have babies?
However, problems with their testicles prevent them from making enough normal sperm to father children. The vast majority of men with Klinefelter syndrome are infertile and can’t father a child the usual way. Options for becoming natural parents are limited, but fertility researchers are working on new treatments.
What does XXY mean?
Klinefelter syndrome, also known as the XXY condition, is a term used to describe males who have an extra X chromosome in most of their cells. About one of every 500 males has an extra X chromosome, but many don’t have any symptoms.
How is Klinefelter’s diagnosed?
Blood or urine samples can reveal abnormal hormone levels that are a sign of Klinefelter syndrome. Chromosome analysis. Also called karyotype analysis, this test is used to confirm a diagnosis of Klinefelter syndrome. A blood sample is sent to the lab to check the shape and number of chromosomes.
Who is affected by Klinefelter syndrome?
Klinefelter syndrome affects about 1 in 650 newborn boys. It is among the most common sex chromosome disorders, which are conditions caused by changes in the number of sex chromosomes (the X chromosome and the Y chromosome).