What is Down Syndrome?
Down syndrome (sometimes called Down’s syndrome) is a condition in which a child is born with an extra copy of their 21st chromosome — hence its other name, trisomy 21. This causes physical and mental developmental delays and disabilities.
Many of the disabilities are lifelong, and they can also shorten life expectancy. However, people with Down syndrome can live healthy and fulfilling lives. Recent medical advances, as well as cultural and institutional support for people with Down syndrome and their families, provides many opportunities to help overcome the challenges of this condition.
Types of Down Syndrome
There are three types of Down syndrome:
- Trisomy 21
Trisomy 21 means there’s an extra copy of chromosome 21 in every cell. This is the most common form of Down syndrome.
Mosaicism occurs when a child is born with an extra chromosome in some but not all of their cells. People with mosaic Down syndrome tend to have fewer symptoms than those with trisomy 21.
In this type of Down syndrome, children have only an extra part of chromosome 21. There are 46 total chromosomes. However, one of them has an extra piece of chromosome 21 attached.
Causes of Down Syndrome
In all cases of reproduction, both parents pass their genes on to their children. These genes are carried in chromosomes. When the baby’s cells develop, each cell is supposed to receive 23 pairs of chromosomes, for 46 chromosomes total. Half of the chromosomes are from the mother, and half are from the father.
In children with Down syndrome, one of the chromosomes doesn’t separate properly. The baby ends up with three copies, or an extra partial copy, of chromosome 21, instead of two. This extra chromosome causes problems as the brain and physical features develop.
According to the National Down Syndrome Society (NDSS), about 1 in 700 babies in the United States is born with Down syndrome. It’s the most common genetic disorder in the United States.
Risk factor of Down Syndrome
Certain parents have a greater risk of giving birth to a child with Down syndrome. According to the Centers for Disease and Prevention, mothers aged 35 and older are more likely to have a baby with Down syndrome than younger mothers. The risk increases the older the mother is.
Research shows that paternal age also has an effect. One 2003 study found that fathers over 40 had twice the risk of having a child with Down syndrome.
Other parents who are at greater risk of having a child with Down syndrome include:
- people with a family history of Down syndrome
- people who carry the genetic translocation
It’s important to remember that no one of these factors mean that you’ll definitely have a baby with Down syndrome. However, statistically and over a large population, they can put you at higher risk.
Symptoms of Down Syndrome
Though the likelihood of carrying a baby with Down syndrome can be estimated by screening during pregnancy, you won’t experience any symptoms of carrying a child with Down syndrome.
At birth, babies with Down syndrome usually have certain characteristic signs, including:
- flat facial features
- small head and ears
- short neck
- bulging tongue
- eyes that slant upward
- a typically shaped ears
- poor muscle tone
An infant with Down syndrome can be born an average size, but will develop more slowly than a child without the condition.
People with Down syndrome usually have some degree of developmental disability, but it’s often mild to moderate. Mental and social development delays may mean that the child could have:
- impulsive behavior
- poor judgment
- short attention span
- slow learning capabilities
Complications of Down Syndrome
These may include:
- congenital heart defects
- hearing loss
- poor vision
- cataracts (clouded eyes)
- hip problems, such as dislocations
- chronic constipation
- sleep apnea (interrupted breathing during sleep
- dementia (thought and memory problems)
- hypothyroidism (low thyroid function)
- late tooth growth, causing problems with chewing
- Alzheimer’s disease later in life
People with Down syndrome are also more prone to infection. They may struggle with respiratory infections, urinary tract infections, and skin infections.
Screening for Down syndrome during pregnancy
Screening for Down syndrome is offered as a routine part of prenatal care in the United States. If you’re a woman over 35, your baby’s father is over 40, or there’s a family history of Down syndrome, you may want to get an evaluation.
An ultrasound evaluation and blood tests can look for Down syndrome in your fetus. These tests have a higher false-positive rate than tests done at later pregnancy stages. If results aren’t normal, your doctor may follow up with an amniocentesis after your 15th week of pregnancy.
An ultrasound and quadruple marker screen (QMS) test can help identify Down syndrome and other defects in the brain and spinal cord. This test is done between 15 and 20 weeks of pregnancy.
If any of these tests aren’t normal, you’ll be considered at high risk for birth defects.
Additional prenatal tests
Your doctor may order additional tests to detect Down syndrome in your baby. These may include:
- Amniocentesis: Your doctor takes a sample of amniotic fluid to examine the number of chromosomes your baby has. The test is usually done after 15 weeks.
- Chorionic villus sampling (CVS): Your doctor will take cells from your placenta to analyze fetal chromosomes. This test is done between the 9th and 14th week of pregnancy. It can increase your risk of a miscarriage, but according to the Mayo Clinic, only by less than 1 percent.
- Percutaneous umbilical blood sampling (PUBS, or cordocentesis): Your doctor will take blood from the umbilical cord and examine it for chromosomal defects. It’s done after the 18th week of pregnancy. It has a higher risk of miscarriage, so it’s performed only if all other tests are uncertain.
Some women choose not to undergo these tests because of the risk of miscarriage. They’d rather risk having a child with Down syndrome than lose the pregnancy.
Tests at birth
At birth, your doctor will:
- perform a physical examination of your baby
- order a blood test called a karyotype to confirm Down syndrome
Treatment of Down Syndrome
There’s no cure for Down syndrome, but there’s a wide variety of support and educational programs that can help both people with the condition and their families. The NDSS is just one place to look for programs nationwide.
Available programs start with interventions in infancy. Federal law requires that states offer therapy programs for qualifying families. In these programs, special education teachers and therapists will help your child learn:
- sensory skills
- social skills
- self-help skills
- motor skills
- language and cognitive abilities
Children with Down syndrome often meet age-related milestones. However, they may learn more slowly than other children.
School is an important part of the life of a child with Down syndrome, regardless of intellectual ability. Public and private schools support people with Down syndrome and their families with integrated classrooms and special education opportunities. Schooling allows valuable socialization and helps students with Down syndrome build important life skills.