Klinefelter syndrome is the presence of an extra X chromosome in a male.
Humans have 46 chromosomes. Chromosomes contain all of your genes and DNA, the building blocks of the body. The two sex chromosomes determine if you become a boy or a girl. Females normally have two of the same sex chromosomes, written as XX. Males normally have an X and a Y chromosome (written as XY).
Klinefelter syndrome is one of a group of sex chromosome problems. It results in males who have at least one extra X chromosome. Usually, this occurs due to one extra X (written as XXY).
Klinefelter syndrome is found in about 1 out of every 500 - 1,000 newborn males. Women who have pregnancies after age 35 are slightly more likely to have a boy with this syndrome than younger women.
The most common symptom is infertility. Other symptoms may include:
Adults may come to the doctor because of infertility. School-age children may be brought in to because of learning problems.
The following tests may be performed:
Testosterone therapy may be prescribed. This can help:
Most men with this syndrome are not able to father children. However, some men have been able to have children. An infertility specialist may be able to help.
Most patients have a normal, productive life.
The syndrome increases the risk of:
Enlarged teeth with a thinning surface (taurodontism) is very common in Klinefelter syndrome. It can be diagnosed by dental x-rays.
Call for an appointment with your health care provider if a boy does not develop secondary sexual characteristics at puberty.
A genetics counselor can provide information about this condition, and help explain abnormal chromosome findings and possible complications. The counselor will also be familiar with local and national support groups.
An endocrinologist and infertility specialist may also be helpful.
47 X-X-Y syndrome