Down syndrome is a genetic disorder. It is also called trisomy 21. It includes certain birth defects, learning problems, and facial features. A child with Down syndrome also may have heart defects and problems with vision and hearing. How severe or mild these problems are varies from child to child.
Down syndrome is one of the most common genetic birth defects. It affects about 1 in 700 babies. Adults with Down syndrome may live about 60 years, but this can vary.
When a baby is conceived, a normal egg cell and normal sperm cell start with 46 chromosomes. The egg and sperm cells then divide in half. The egg and sperm cells then have 23 chromosomes each. When a sperm with 23 chromosomes fertilizes an egg with 23 chromosomes, the baby will then have a complete set of 46 chromosomes. Half are from the father and half are from the mother.
But sometimes an error occurs when the 46 chromosomes are being divided in half. An egg or sperm cell may keep both copies of chromosome number 21, instead of just 1 copy. If this egg or sperm is fertilized, then the baby will have 3 copies of chromosome number 21. This is called trisomy 21.
Sometimes the extra number 21 chromosome or part of it is attached to another chromosome in the egg or sperm. This may cause translocation Down syndrome. This is the only form of Down syndrome that may be inherited from a parent.
A rare form is called mosaic trisomy 21. This is when an error in cell division happens after the egg is fertilized. People with this syndrome have both normal cells and some cells with an extra chromosome number 21.
A mother’s age at her child’s birth is a factor linked to the risk of having a baby with Down syndrome. This risk increases with each year of age, especially after age 35. But younger women are more likely to have babies than older women. Therefore, most babies with Down syndrome are born to women younger than 35.
Symptoms can occur a bit differently in each child. They can include:
Eyes that slant up
Small ears that may fold over slightly at the top
Small mouth that makes the tongue seem large
Small nose with a flattened bridge
Small hands with short fingers
Two instead of 3 palm creases, including one across the palm and one around the base of the thumb
Most children with Down syndrome will have some but not all of these features.
Down syndrome can also include:
Blood conditions, such as leukemia, and risk for infections
Chromosome problems such as Down syndrome can often be diagnosed before birth. Screening tests are often done first. These often combine a blood test with an ultrasound. A screening test tells you and your healthcare provider if you have a greater or lesser chance of having Down Syndrome. They don't make a diagnosis. A diagnostic test is more invasive and risky. But it generally can find the disorder.
The screening ultrasound looks at the amount of amniotic fluid present. Extra fluid means there is a problem. The blood test looks at many substances in the blood, such as MS-AFP, Triple Screen, and Quad-screen, to show a possible risk. These tests look at various levels of certain substances such as alpha-fetoprotein, human chorionic gonadotropin, estriol to determine risk. Fetal ultrasound during pregnancy can also show the possibility of Down syndrome. But ultrasound is not 100% accurate. Problems from Down syndrome may not be seen with ultrasound.
Diagnostic tests are done by looking at cells in the amniotic fluid or from the placenta. These tests include:
Chorionic villus sampling. This test examines cells from the placenta.
Amniocentesis. This tests the fluid from the sac surrounding the baby (amniotic fluid).
Percutaneous umbilical blood sampling. This tests blood from the umbilical cord.
All 3 of these tests look for characteristic changes in the chromosomes that occur in a Down syndrome diagnosis.
After birth, your baby may be diagnosed with a physical exam. The healthcare provider may also take a blood sample. This is checked in a lab to find the extra chromosome.
There is no cure for Down syndrome. But a child with Down syndrome may need treatment for problems such as:
Heart defects. About half of babies with Down syndrome have heart defects. Some defects are minor. These can be treated with medicines or they will fix themselves on their own. Others may need surgery. All babies with Down syndrome should have an echocardiogram (heart ultrasound) and be looked at by a pediatric cardiologist. This exam and test should be done shortly after birth. This is so that any heart defects can be found and treated correctly.
Intestinal problems. Some babies with Down syndrome are born with intestinal problems that need surgery.
Vision problems. Common problems include crossed eyes, nearsightedness or farsightedness, and cataracts. Most eyesight problems can be made better with eyeglasses, surgery, or other treatments. Your child should see an eye doctor (pediatric ophthalmologist) before they turn 1 year old.
Hearing loss. This is caused by fluid in the middle ear, a nerve defect, or both. Your child should get regular hearing tests so any problems can be treated early. This will help with language development.
Other health problems. Children with Down syndrome may have thyroid problems and leukemia. They also tend to have many colds, as well as bronchitis and pneumonia. Your child should get regular medical care and stay up to date on vaccines.
Learning problems. These vary widely from child to child. They can be mild, moderate, or severe. But most learning problems are mild to moderate. Many children will receive early intervention and special education.
Some people claim that giving high-dose vitamins to children with Down syndrome will improve their learning and development problems. No studies have proved that this works.
Talk with your child’s healthcare providers about the risks, benefits, and possible side effects of all treatments.
Complications of Down syndrome vary depending on the body organ affected and the severity of the problem. Problems include certain birth defects, learning problems, and facial features. A child with Down syndrome also may have heart defects and problems with vision and hearing. How severe the complications are varies from child to child. Treatment will also vary depending on the body organ affected and the severity of the problem. Your child’s healthcare provider will discuss treatment options with you.
Researchers don’t know how to prevent the chromosome errors that cause this disorder. There is no reason to believe parents can do anything to cause or prevent Down syndrome in their child.
For women who have had one child with Down syndrome, the chance of having another baby with Down syndrome depends on several things. Age is one factor. Most babies with Down syndrome are born to women younger than 35. This is because women under 35 have more babies than women over 35.
Your healthcare provider may refer you to a genetic counselor. This expert can explain the results of chromosome tests in detail. They can talk about risks for future pregnancies and what tests are available to diagnose chromosome problems before a baby is born.
Some medical organizations advise that all pregnant women of any age be offered screening for Down syndrome. Talk with your healthcare provider about this prenatal screening test.
Children with Down syndrome can often do most things that any young child can do. They can walk, talk, dress themselves, and be toilet trained. But they often do these things at a later age than other children. The exact ages of these development milestones is different for each child. Early intervention programs that begin when a child is a baby can help the child reach their potential.
A child with Down syndrome can go to school. Special programs beginning in the preschool years help children with Down syndrome develop skills as fully as possible. Many children are helped with early intervention and special education. They can also enter a regular classroom. Many children will learn to read and write. They can take part in childhood activities, both at school and in their community.
Your child may need physical, occupational, and speech therapy to help with their development. Talk with your child's healthcare provider, other families, and national Down syndrome support agencies to learn what to expect with Down syndrome. You can also learn what may be helpful in raising a child with Down syndrome.
Special work programs are designed for adults with Down syndrome. Many adults with this disorder can hold regular jobs. More and more adults with Down syndrome live semi-independently in community group homes. They take care of themselves, do household chores, develop friendships, do leisure activities, and work in their communities.
Some people with Down syndrome marry. Most men with Down syndrome can't father a child. In any pregnancy, a woman with Down syndrome has a 1 in 2 chance of conceiving a child with Down syndrome. Many of the pregnancies are miscarried.
Call the healthcare provider if your child has:
Symptoms that don’t get better, or get worse
Down syndrome (trisomy 21) is a genetic disorder. It includes certain birth defects, learning problems, and facial features. A child with Down syndrome also may have heart defects and problems with vision and hearing.
A mother’s age at her child’s birth is the only factor linked to the risk of having a baby with Down syndrome. This risk increases with each year of age, especially after age 35.
There is no reason to believe parents can do anything to cause or prevent Down syndrome in their child. Researchers don’t know how to prevent the chromosome errors that cause this disorder.
Down syndrome can often be diagnosed before birth. After birth, your baby may be diagnosed with a physical exam. The healthcare provider may also take a blood sample.
There is no cure for Down syndrome, but treatment is available to help your child.
Your child may need physical, occupational, and speech therapy to help with their development. Many children are helped with early intervention and special education.
Tips to help you get the most from a visit to your child’s healthcare provider:
Know the reason for the visit and what you want to happen.
Before your visit, write down questions you want answered.
At the visit, write down the name of a new diagnosis, and any new medicines, treatments, or tests. Also write down any new instructions your provider gives you for your child.
Know why a new medicine or treatment is prescribed and how it will help your child. Also know what the side effects are.
Ask if your child’s condition can be treated in other ways.
Know why a test or procedure is recommended and what the results could mean.
Know what to expect if your child does not take the medicine or have the test or procedure.
If your child has a follow-up appointment, write down the date, time, and purpose for that visit.
Know how you can contact your child’s provider after office hours. This is important if your child becomes ill and you have questions or need advice.