- What is the most common treatment for Klinefelters?
- What is the life expectancy of a person with Klinefelter syndrome?
- Who is most likely to get Klinefelter’s syndrome?
- Is Klinefelter syndrome classed as a disability?
- What is another name for Klinefelter syndrome?
- What is super male syndrome?
- When can Klinefelter syndrome be detected?
- What does a person with Klinefelter syndrome look like?
- What is the main cause of Klinefelter?
- Are all Klinefelter’s infertile?
- How do you test for XXY?
What is the most common treatment for Klinefelters?
Treatment of Klinefelter Syndrome One common treatment is testosterone replacement therapy.
It can start at puberty and can spur typical body changes, such as facial hair and a deeper voice.
It can also help with penis size and stronger muscles and bones, but it won’t affect testicle size or fertility..
What is the life expectancy of a person with Klinefelter syndrome?
According to research, Klinefelter syndrome can shorten your life expectancy up to two years. However, you can still live a long, full life with this condition.
Who is most likely to get Klinefelter’s syndrome?
Klinefelter syndrome results when a boy is born with at least 1 extra X chromosome. This is written as XXY. Klinefelter syndrome occurs in about 1 out of 500 to 1,000 baby boys. Women who get pregnant after age 35 are slightly more likely to have a boy with this syndrome than younger women.
Is Klinefelter syndrome classed as a disability?
Social Security Benefits If you or your dependent(s) are diagnosed with Klinefelter Syndrome and experience any of these symptoms, you may be eligible for disability benefits from the U.S. Social Security Administration.
What is another name for Klinefelter syndrome?
Klinefelter syndrome (KS), also known as 47,XXY is a syndrome where a male has an additional copy of the X chromosome. The primary features are infertility and small poorly functioning testicles. Often, symptoms are subtle and subjects do not realize they are affected.
What is super male syndrome?
XYY syndrome is a rare chromosomal disorder that affects males. It is caused by the presence of an extra Y chromosome. Males normally have one X and one Y chromosome. However, individuals with this syndrome have one X and two Y chromosomes. Affected individuals are usually very tall.
When can Klinefelter syndrome be detected?
How is Klinefelter syndrome diagnosed? Klinefelter syndrome usually is not diagnosed until the time of puberty. At this point, the boy’s testicles fail to grow, and you may start to notice other symptoms.
What does a person with Klinefelter syndrome look like?
Longer legs, shorter torso and broader hips compared with other boys. Absent, delayed or incomplete puberty. After puberty, less muscle and less facial and body hair compared with other teens. Small, firm testicles.
What is the main cause of Klinefelter?
Klinefelter syndrome is caused by an additional X chromosome. This chromosome carries extra copies of genes, which interfere with the development of the testicles and mean they produce less testosterone (male sex hormone) than usual.
Are all Klinefelter’s infertile?
Klinefelter syndrome is one of the leading causes of male infertility. Approximately 3% of all infertile men have Klinefelter syndrome and 14% of non-obstructive azoospermic men have Klinefelter syndrome. Klinefelter syndrome is a chromosomal condition that affects male physical and cognitive development.
How do you test for XXY?
How Is Klinefelter Syndrome Diagnosed?Hormone testing, which is usually done by taking a blood sample to check for abnormal hormone levels.A chromosome analysis, or karyotype, which is usually done on a blood sample. This test checks the number of chromosomes to see if the XXY syndrome is present.