Exams and Tests
Klinefelter syndrome can be identified before birth
(prenatally) through
amniocentesis or
chorionic villus sampling (CVS). It also can be
diagnosed in childhood, during puberty, or in adulthood by a medical history,
physical exam, and a chromosome test called a
karyotype. Other lab tests, such as hormone tests or a
semen analysis, may be done if Klinefelter syndrome is
suspected.
Prenatal testing
Amniocentesis and chorionic villus sampling (CVS) are not routine
prenatal tests. They usually are done when there is a family history of
genetic disorders (such as Klinefelter syndrome) or
when the mother is older than 35.
Testing in childhood or during puberty
Klinefelter syndrome usually is not diagnosed before the preteen
years because there are no symptoms or because symptoms go unnoticed until
puberty. However, a doctor may suspect Klinefelter
syndrome when a young boy has difficulty learning to talk, read, or write.
During puberty, some males may be suspected of having Klinefelter
syndrome, including those who:
- Are taller than other males in their family
and have long legs.
- Have small testicles that do not increase in
size as puberty progresses.
- Have enlarged breast tissue that
persists for more than 2 years.
- Have learning or social problems
(such as lacking self-confidence and being shy, immature, or
dependent).
- Have mild mental retardation. Klinefelter syndrome is
present in about 1% of males with mental retardation.3
Tests for Klinefelter syndrome during childhood or puberty
usually include a medical history, physical exam, and karyotype.
Adult testing
Klinefelter syndrome may not be diagnosed until adulthood when a
man seeks medical care to determine the cause of his
infertility. About 3% of infertile men have
Klinefelter syndrome.3 Tests include a medical
history, physical exam, and karyotype. A man may also have hormone tests and a
semen analysis.