Topic Overview
What is Klinefelter syndrome?
Klinefelter syndrome is a
genetic disorder that affects males. Klinefelter
syndrome occurs when a boy is born with one or more extra X
chromosomes. Most males have one Y and one X
chromosome. Having extra X chromosomes can cause a male to have some physical
traits unusual for males.
Many men with an extra X chromosome are not aware that they have
it, and they lead normal lives. Males with Klinefelter syndrome may be
described as XXY males or males with XXY syndrome. Klinefelter syndrome occurs
in about 1 in 1,000 males.
What causes Klinefelter syndrome?
The presence of an extra X chromosome in males most often occurs
when cells split unevenly to produce eggs. But it can also occur when cells
split unevenly to produce sperm.
What are the symptoms?
Many men with Klinefelter syndrome do not have obvious symptoms.
Others have sparse body hair, enlarged breasts, and wide hips. In almost all
men the testicles remain small. In some men the penis does not reach adult
size. Their voice may not be as deep. They usually cannot father children, but
they can have a normal sex life.
Some boys with Klinefelter syndrome have language and learning
problems.
See a picture of a
man with
Klinefelter syndrome
.
How is Klinefelter syndrome diagnosed?
Klinefelter syndrome usually is not diagnosed until around ages
11 to 12, when boys often begin
puberty. At this point, the boy's testicles fail to
grow normally and you may start to notice other symptoms.
To find out if your son has Klinefelter syndrome, your doctor
will ask questions about his past health, do a physical exam, and order a
chromosome test called a
karyotype.
How is it treated?
Males with Klinefelter syndrome can be given testosterone, a
hormone needed for sexual development. If treatment is started around the age
of puberty, it can help a boy have more normal body development.
Speech therapy and educational support can help boys who have
language or learning problems.
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