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Klinefelter syndromeDefinitionKlinefelter syndrome is a condition that occurs in men as a result of an extra X chromosome. The most common symptom is infertility. Alternative Names 47 X-X-Y syndrome CausesHumans have 46 chromosomes, which contain all of a person’s genes and DNA. Two of these chromosomes, the sex chromosomes, determine a person’s gender. Both of the sex chromosomes in females are called X chromosomes. (This is written as XX.) Males have an X and a Y chromosome (written as XY). The two sex chromosomes help a person develop fertility and the sexual characteristics of their gender. Klinefelter syndrome results in males who have at least one extra X chromosome. Usually, this occurs as a result of 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. Exams and TestsThe patient may have the following signs:
Adults may come to the doctor because of infertility. School-age children may be brought in to evaluate learning disabilities. The following test results may be found:
TreatmentTestosterone therapy can achieve the following:
Most patients are not able to father children. However, there are some cases of men with an extra X fathering healthy offspring, sometimes with the aide of infertility specialists. Support GroupsThe Klinefelter Syndrome Association can be reached at PO Box 119, Roseville, CA, 95678-0119. Outlook (Prognosis)Most patients can expect a normal, productive life. Social and educational supports can help patients reach their potential. Possible ComplicationsThe syndrome is associated with an increased risk of breast cancer, extragonadal germ cell tumor (a rare tumor), lung disease, varicose veins, and osteoporosis. There is also an increased risk for autoimmune disorder such as lupus, rheumatoid arthritis, and Sjogren's syndrome. Learning disabilities are common, despite normal or high IQ. The risks of dyslexia, attention deficient hyperactivity disorder, and depression may be higher. Taurodontism, which is when the teeth have enlarged pulp and surface thinning, is very common in Klinefelter syndrome. It can be diagnosed by dental x-rays. When to Contact a Medical ProfessionalCall for an appointment with your health care provider if a boy fails to develop secondary sexual characteristics at puberty A genetics counselor can help evaluate or explain abnormal chromosome findings. The patient may also wish to consult with an endocrinologist and infertility specialist.
Review Date:
10/27/2004 Reviewed By: Celeste Krauss, M.D., Board Certified Clinical Genetics, Clinical Cytogenetics, Pediatrics and a Founding Fellow, of the American College of Medical Genetics. Review provided by VeriMed Healthcare Network. The information provided herein should not be used during any medical emergency or for the diagnosis or treatment of any medical condition. A licensed medical professional should be consulted for diagnosis and treatment of any and all medical conditions. Call 911 for all medical emergencies. Links to other sites are provided for information only -- they do not constitute endorsements of those other sites. © 1997-
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