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Klinefelter syndrome

Read about Klinefelter syndrome - a condition in which male babies are born with an extra X chromosome. Find out about the symptoms, causes and treatments.

5 April 2023

Introduction

Klinefelter syndrome (sometimes called Klinefelter's, KS or XXY) is where boys and men are born with an extra X chromosome.

Chromosomes are packages of genes found in every cell in the body. There are 2 types of chromosome, called the sex chromosomes, that determine the genetic sex of a baby. These are named either X or Y.

Usually, a female baby has 2 X chromosomes (XX) and a male has 1 X and 1 Y (XY). But in Klinefelter syndrome, a boy is born with an extra copy of the X chromosome (XXY).

The X chromosome is not a "female" chromosome and is present in everyone. The presence of a Y chromosome denotes male sex.

Boys and men with Klinefelter syndrome are still genetically male, and often will not realise they have this extra chromosome, but occasionally it can cause problems that may require treatment.

Klinefelter syndrome does not usually cause any obvious symptoms early in childhood, and even the later symptoms may be difficult to spot.

Many boys and men do not realise they have it.

Possible features, which are not always present, may include:

  • in babies and toddlers – weak muscles and very flexible (hypermobile) joints, learning to sit up, crawl, walk and talk later than usual, being quieter and more passive than usual, having undescended testicles, only one testicle, or a smaller penis
  • in childhood – shyness and low self-confidence, problems with reading, writing, spelling and paying attention, mild dyslexia ↗ or dyspraxia ↗, low energy levels, and difficulty socialising or expressing feelings
  • in teenagers – growing taller than expected for the family (with long arms and legs), broad hips, poor muscle tone and slower than usual muscle growth, reduced facial and body hair that starts growing later than usual, small, firm testes, and enlarged breasts (gynaecomastia ↗) ↗
  • in adulthood – inability to have children naturally (infertility) ↗, low sex drive ↗, small, firm testes, and erection problems.

Many boys and men with Klinefelter syndrome will not be significantly affected and can live normal, healthy lives.

Infertility tends to be the main problem, although there are treatments that can help.

But men with Klinefelter syndrome are at a slightly increased risk of developing other health problems, including:

These problems can usually be treated if they do occur and testosterone replacement therapy may help reduce the risk of some of them.

Klinefelter syndrome is caused by an additional X chromosome.

This chromosome carries extra copies of genes, which may interfere with the development of the testicles and mean they produce less testosterone (male sex hormone) than usual.

The extra genetic information may either be carried in every cell in the body or it may only affect some cells (known as mosaic Klinefelter syndrome).

Klinefelter syndrome is not directly inherited – the additional X chromosome occurs as a result of either the mother's egg or the father's sperm having the extra X chromosome (an equal chance of this happening in either), so after conception the chromosome pattern is XXY rather than XY.

This change in the egg or sperm seems to happen randomly. If you have a son with the condition, the chances of this happening again are very small.

The risk of a woman having a son with Klinefelter syndrome may be slightly higher if the mother or father are older.

See your GP if you have concerns about your son's development or you notice any symptoms of Klinefelter syndrome in yourself or your son.

Early diagnosis and treatment can help prevent health problems in the future.

Treatment can help reduce some of the symptoms if necessary.

In many cases, it's only detected if a man with the condition undergoes fertility tests.

Your GP may suspect Klinefelter syndrome after a physical examination and may suggest sending off a sample of blood to check reproductive hormone levels.

The diagnosis can be confirmed by checking a sample of blood for the presence of the extra X chromosome.

Klinefelter syndrome can also be picked up as part of some screening tests during pregnancy.

There's no cure for Klinefelter syndrome, but some of the problems associated with the condition can be treated if necessary.

Possible treatments include:

Testosterone replacement therapy (TRT)

TRT involves taking medicines containing testosterone. It can be taken in the form of gels or tablets in children, or given as gel or injections in adult men.

TRT may be considered once puberty begins and may help with the development of a deep voice, facial and body hair, an increase in muscle mass, reduction in body fat, and improvement in energy. There is also evidence that it can help with learning and behavioural problems.

You should see a specialist in children's hormones (a paediatric endocrinologist) at this time.

Long-term treatment during adulthood may also help with several other problems associated with Klinefelter syndrome – including osteoporosis, low mood, reduced sex drive, low self-esteem and low energy levels – although it cannot reverse infertility.

TRT may be stopped during fertility treatment, or not started until after fertility treatment.

Treatment with TRT will be monitored by your care team as it can cause side effects and health issues.

Lifestyle changes

Leading a healthy lifestyle, including eating a healthy diet and exercising regularly, can help reduce your chances of getting conditions like type 2 diabetes, osteoporosis, and cardiovascular disease.

It can also help with your mental health, including depression and anxiety.

Try to quit smoking and try to not drink more alcohol than the recommended limit of 14 units of alcohol a week, spread across 3 days.

If you or your son has been diagnosed with Klinefelter syndrome, you might find it useful to find out more about it and get in touch with others affected by it.

The following websites may be able to help: