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Turner Syndrome

Turner Syndrome

What are monosomies?

Most people have 46 chromosomes in their cells. Monosomy means that a person is missing one member of a pair of chromosomes. Instead of 46, the person has only 45 chromosomes. For example, if a baby is born with only one X sex chromosome, rather than the usual pair (either two X's or one X and one Y sex chromosome), the baby would have monosomy X. Monosomy X is also known as Turner syndrome.

What is Turner syndrome?

Turner syndrome is a genetic disorder that occurs in girls. It causes them to be shorter than others. They also don’t go through normal puberty as they grow into adulthood. The seriousness of these problems varies from girl to girl. A child with Turner syndrome may also have other health problems. These include problems of the heart or kidneys. Many of the health problems affecting girls with Turner syndrome can be managed or fixed with treatment. Turner syndrome occurs in about 1 in 2,000 to 2,500 girl babies.

What causes Turner syndrome?

When a baby is conceived, the egg cell of the mother and the sperm cell of the father start out with the usual number of 46 chromosomes. The egg and sperm cells both divide, so that the chromosome number is half of 46. The egg and the sperm cells then have 23 chromosomes each. When a sperm with 23 chromosomes fertilizes an egg with 23 chromosomes, the baby will have a complete set of 46 chromosomes. Half are from the father and half are from the mother.

Sometimes an error occurs when an egg or sperm cell is forming, causing it to have a missing sex chromosome. When this cell can’t give a sex chromosome to the embryo, the embryo ends up with only one X sex chromosome. This causes Turner syndrome.

The missing sex chromosome error can occur in either the mother's egg cell or the father's sperm cell. But it is usually an error that happened randomly when the father's sperm cell was forming.

About half of all cases of Turner syndrome happen because of full monosomy X. Others have a mosaic pattern. This means the body’s cells have 2 or more chromosome patterns. A small portion of cases result from having the normal number of 46 chromosomes, but with part of the X chromosome missing. When only part of an X chromosome is missing (deletion), a girl with the syndrome will usually have milder features. The features of Turner syndrome that are present depend on which part of the X chromosome is missing.

What are the signs and symptoms of Turner syndrome?

About half of girls born with Turner syndrome will have puffy hands and feet at birth. They will also have a wide neck with webbing. During a pregnancy, the doctor may have seen a structure called a cystic hygroma during fetal ultrasound. Cystic hygromas are fluid-filled sacs at the base of the neck. They often go away before birth. But sometimes the sac is there when the baby is born.

Girls with Turner syndrome usually have:

  • A low hairline at the back of the neck

  • Small differences in the shape and position of the ears

  • Broad chest with widely spaced nipples

  • More small brown moles (nevi) on the skin than normal

  • Deep-set nails 

Being shorter than normal is the most visible feature of Turner syndrome. The average adult height of a woman with Turner syndrome is 4 feet, 8 inches.

Most women with Turner syndrome are born with poorly formed or missing ovaries. Ovaries make estrogen, and without it, a girl with Turner syndrome will not develop sexually. The usual signs of puberty—breast development, menstruation, and growth of pubic hair and hair elsewhere on the body—don’t happen unless the girl is given hormone therapy. A girl with the syndrome will usually be infertile as an adult.

Other common problems with Turner syndrome affect the heart, kidney, and thyroid. About 1 in 10 girls with Turner syndrome is born with coarctation of the aorta. This means the main artery that leaves the heart is narrowed. This problem sometimes needs to be corrected surgically.

Other problems seen in Turner syndrome include:

  • Feeding problems during infancy

  • Middle ear infections

  • Skeletal problems

  • Cubitus valgus. This means that when a girl stands with her arms at her side, her elbows will be slightly bent. She can’t keep her arms perfectly straight at her side.

  • Diabetes

  • Dry skin

  • High blood pressure

  • Small jaw

  • Narrow top of the inside of the mouth

Girls with Turner syndrome generally have normal intelligence. They tend to score higher on their verbal IQ than their nonverbal IQ. They may have problems in the areas of spatial perception. They may also have certain learning disabilities.

How is Turner syndrome diagnosed?

If the healthcare provider thinks that your newborn may have Turner syndrome, he or she will usually take a small sample of your baby’s blood. The lab will look at the sample to see if the sex chromosome is missing.

Sometimes a girl with Turner syndrome doesn’t have any problems as an infant or child. It’s only when she doesn’t go through puberty or is shorter than her peers that her doctor may suspect Turner syndrome.

Chromosome problems such as Turner syndrome can often be diagnosed before birth. This is done by looking at cells in the amniotic fluid or from the placenta. This can also be done by looking at the amount of fetal DNA in the mother's blood (noninvasive prenatal screening).

Fetal ultrasound during pregnancy can also show the possibility of Turner syndrome. But ultrasound is not 100% accurate. Many babies with Turner syndrome may look the same on ultrasound as those without Turner syndrome.

A chromosome analysis done on a blood sample or on cells from the amniotic fluid or placenta is very accurate.

What is the risk of having another child with Turner syndrome?

In general, a woman who has a child with Turner syndrome is not at increased risk of having another baby with the condition.

After birth, the doctor usually takes a blood sample from a baby suspected of having Turner syndrome. The lab does a chromosome analysis (karyotype). This confirms the physical findings of Turner syndrome and shows the chromosome problem. Your doctor may explain the results of the test to you. Or your doctor may refer you to a genetic doctor or genetic counselor. This expert can explain the results of chromosome tests, as well as tests available to diagnose chromosome problems before a baby is born.

Can Turner syndrome be cured or prevented?

There is no cure for Turner syndrome. But many of the more serious problems can be treated. For example, growth hormone and androgen therapy can increase the final adult height of a girl with the syndrome. A girl can also take hormone therapy to develop secondary sex traits. Surgery can fix coarctation of the aorta, if needed. And medicines are available to treat high blood pressure, diabetes, and thyroid problems. A woman with Turner syndrome can have children by using donor eggs. 

Reviewed Date: 11-01-2016

Turner Syndrome

Disclaimer: This information is not intended to substitute or replace the professional medical advice you receive from your child's physician. The content provided on this page is for informational purposes only, and was not designed to diagnose or treat a health problem or disease. Please consult your child's physician with any questions or concerns you may have regarding a medical condition.