Klinefelter syndrome (KS)

What is Klinefelter syndrome (KS)?

Klinefelter syndrome (also known as XXY syndrome) is a genetic syndrome that is found only in males. Boys with Klinefelter Syndrome are born with an extra sex chromosome in their cells.

Typically, females have two X chromosomes, while males have one X and one Y chromosome. In males with Klinefelter syndrome, there are two X chromosomes and one Y chromosome (XXY). Rarely there are additional X chromosomes that are present in the cells (XXXY).

As the boys develop into adolescents (12-17 years of age), their condition becomes more apparent, as they can be taller than other boys their age, with disproportionally long arms and legs.

Klinefelter syndrome (KS) was first described by Dr. Harry Klinefelter and his colleagues in 1942. It was later identified as a genetic condition in 1959 by researcher Patricia A. Jacobs.

What are the signs and symptoms of Klinefelter syndrome (KS)?

Males with Klinefelter syndrome typically demonstrate symptoms during the onset of puberty, including:

• Breast growth

• Less than average body and facial hair

• Lower sexual interest

• Narrow shoulders

• Smaller testes

• Smaller penis

• Wide hips

In addition to physical symptoms, boys with Klinefelter Syndrome can also have language, emotional or learning delays. As adult males, they can also be affected by infertility due to low sperm count.

What are the causes of Klinefelter syndrome (KS)?

While Klinefelter syndrome is congenital (present at birth), is not hereditary (passed down in families). It occurs during fetal development when the chromosomes divide.