Klinefelter syndrome specialists work to explore the symptoms that only affect males who have been born with this genetic condition. Klinefelter syndrome is a genetic condition caused when males are born with an extra chromosome. Some specialists refer to Klinefelter syndrome as XXY because of the addition of a second X chromosome in males. Some males are born with some cells containing an extra chromosome, while others are born with an extra chromosome in each of the 23 traditional pairs.
Identifying Klinefelter Syndrome in Infants
One of the issues with XXY syndrome is the lack of noticeable symptoms. Before starting testosterone deficiency treatment, Klinefelter syndrome needs to be identified. Infants are usually born with weaker muscles and a quiet personality. Infants often suffer speech delays and take longer to sit up and walk.
Klinefelter Syndrome Symptoms
Many cases of Klinefelter syndrome go unnoticed in babies and only become apparent as a child grows toward puberty. The common signs and symptoms of Klinefelter syndrome include a taller body with broad hips and longer limbs. The genetic differences between those with Klinefelter syndrome and those without include low energy levels and smaller sexual organs. XXY syndrome only affects males and causes delayed or incomplete puberty.
How to Treat Klinefelter Syndrome
Different tests are used throughout childhood and the teenage years to check for hormonal and chromosomal changes. Most patients are treated through testosterone deficiency treatment. Testosterone is a hormone that helps develop muscles, sexual organ growth, and bone density.
There is much to learn from Klinefelter syndrome specialists, including the symptoms and treatments of this genetic condition. Contact The Focus Foundation at https://thefocusfoundation.org to learn more about Klinefelter Syndrome.