Question

Who is most likely to get klinefelter syndrome?

Answer 1

The average person has 46 chromosomes. All of your genes and DNA, the body's building blocks, are stored in chromosomes. The X and Y chromosomes determine whether you are a boy or a girl. In most cases, girls have two X chromosomes. Boys usually have one X chromosome and one Y chromosome.

Complete answer:
Klinefelter syndrome occurs when a guy is born with at least one extra X chromosome. The shorthand for this is XXY. One in every 500 to 1,000 baby boys has Klinefelter syndrome. Women who become pregnant after the age of 35 are slightly more likely to have a male with this disease than younger women.
Klinefelter syndrome (47, XXY) is caused by an extra X chromosome on an XY background; as a result, only males are affected.
The most prevalent symptom of Klinefelter syndrome is infertility, any of the following symptoms could be present:
Abnormal body proportions (long legs, short trunk, shoulder equal to hip size).
Abnormally large breasts (gynecomastia).
Infertility.
Sexual problems.
Less than normal amount of pubic, armpit, and facial hair.
Small, firm testicles.
Tall height.
Small penis size.

When a guy visits his doctor because of infertility, he may be diagnosed with Klinefelter syndrome. The following tests could be carried out:
1. Karyotyping (checks the chromosomes).
2. Semen count.

Blood tests would be done to check hormone levels, including:
1. Estradiol, a type of estrogen
2. Follicle stimulating hormone
3. Luteinizing hormone
4. Testosterone

Treatment: Treatment has been made more extensive. It's possible that testosterone therapy will be prescribed. This may be useful:
Grow hair on your body, muscles will look better, boost your happiness and self-esteem by improving your concentration, increase your strength and sex drive by increasing your energy and sex drive.

Note:
Down syndrome is a genetic condition produced by an additional whole or partial copy of chromosome 21 due to faulty cell division. Down syndrome is characterised by developmental delays and physical characteristics caused by excess genetic material. Individuals with Down syndrome have varying degrees of intellectual disability and developmental delays. It's the most frequent genetic chromosomal condition in children and the leading cause of learning impairments. It is also known to create other medical issues, such as cardiac and gastrointestinal problems.