Also known as: XXY Syndrome, Extra X Chromosome Condition, Klinefelter's, Male Chromosome Disorder, XXY Condition, Genetic Male Infertility Syndrome
Last Updated: October 31, 2026
Klinefelter syndrome, also known as XXY, is a genetic condition where boys and men are born with an extra X chromosome. Normally, males have one X and one Y chromosome (XY), but in Klinefelter syndrome, they have XXY. This extra chromosome is not directly inherited but occurs randomly during the formation of the egg or sperm. The presence of the extra X chromosome can interfere with the development of the testicles, leading to lower-than-normal production of testosterone, the male sex hormone. This hormonal imbalance can cause a range of symptoms and health issues that vary greatly among individuals. While there is no cure for Klinefelter syndrome, many associated problems can be treated. Management often involves hormone replacement therapy and various supportive therapies to address developmental, physical, and psychological challenges, allowing many men to lead normal, healthy lives.
Explore our range of treatment options for Klinefelter syndrome:
Learn about surgical procedures available for Klinefelter syndrome:
Affects
Boys and men
Prevalence
Relatively common genetic condition
Diagnosis
Blood test for chromosomes
Treatment
Hormone replacement therapy
Consult with our healthcare professionals to discuss your symptoms and treatment options.