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 out of 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 voices 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
male with Klinefelter syndrome
.
How is Klinefelter syndrome diagnosed?
Klinefelter
syndrome usually is not diagnosed until the time of
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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