Down syndrome is a common genetic disorder. It occurs in 1 out of 700-800 live births. Down syndrome causes birth defects, medical problems, and some degree of
intellectual disability.
In fact, down syndrome is the most common genetic cause of mild to moderate intellectual disabilities.
Chromosomes contain the genetic makeup of your body. They occur in 23 pairs within the body. Down syndrome is a problem with chromosome pair 21. There is extra genetic material on the chromosome that may be caused by:
An extra chromosome—This type is called Trisomy 21. This results from an error in cell division in the egg or sperm.Extra chromosomes in some cells—Called Mosaic Trisomy 21.Part of the chromosome has broken off and reattached to another chromosome—Called translocation trisomy. In about one third of individuals, the translocation is inherited from a parent.Factors that increase the chance for Down syndrome include:
Genetics: If either parent is a carrier of Translocation Down syndrome, there is an increased risk.Age: The chance of having a child with Down syndrome increases after a woman reaches age 35.Sex: More boys than girls are born with Down syndrome.History of a previous child with Down syndrome.Infants born with Down syndrome may have some or all of the following physical features:
Muscle hypotonia, low muscle toneFlat facial features, a somewhat depressed nasal bridge and a small noseUpward slanted eyes, small skin folds on the inner corner of the eyesShort neckMisshaped earsWhite spots on the colored part of the eyeSingle skin crease in the palm of the handExcess flexibility in jointsHeart defectsSight and hearing problemsLarge and protruding tongueFifth finger has one flexion furrow instead of twoExcessive space between large and second toe
The degree of medical problems and intellectual disability is different for each person. Talents, abilities, and pace of development will be different too. People with Down syndrome may be born with or develop:
Vision problemsHearing lossHeart defects
Increased incidence of acute
leukemiaFrequent ear infections and increased susceptibility to infection in generalGastrointestinal obstruction (imperforate anus and similar problems)Esophageal atresia or duodenal atresiaSleep problems (eg, blocked airways during sleep, daytime sleepiness, sleep anxiety, sleep walking)
Increased incidence of
dementia
in older ages
Instability of the back bones at the top of the neck, can result in compression injury of the spinal cordUrinary system defectsHigh blood pressure
in the lungs
Seizures
An under-active thyroid (hypothyroidism)
Slow growthLate to sit, walk, toilet trainSpeech problemsObesityEmotional problemsMost of these health problems are treatable. The majority of people born with Down syndrome today have a life expectancy of about 55 years.
Doctors can usually identify a child born with Down syndrome at birth. When Down syndrome is suspected, a blood test will be done to confirm it.
Down syndrome may also be diagnosed before birth. There are screening tests and diagnostic tests to help identify chormosome abnormalities before birth.
A screening test is done to estimate the risk of having a child with Down syndrome. Your doctor will use the results of a variety of blood tests and the mother's age to estimate the risk. Blood tests may include:
Triple screen (Alpha-fetoprotein Plus)Quadruple screenCell-Free Fetal DNA Testing
Screening may be done as early as 11 weeks. It may also include both
ultrasound imaging
and blood screening. There should be a follow-up in the second trimester for those who screen negative.
A small amount of women who have screening will be given false-positive readings. This means the test indicates Down syndrome even when it does not exist.
Diagnostic tests will tell if the fetus actually has Down syndrome. These tests include:
Chorionic villus sampling (CVS)—Usually done between 10 and 12 weeksAmniocentesis—Usually done between 12 and 20 weeks of gestation
Percutaneous umbilical blood sampling (PUBS)—Usually done after 20 weeks
These tests are about 98%-99% accurate. Each test requires that a small piece of tissue be removed from the placenta or umbilical cord. This creates a small risk of
miscarriage
with these tests.
There is no cure for Down syndrome.
Treatment may be needed for severe problems or to help with developmental delays. Living at home and receiving special therapy helps children with Down syndrome achieve their full potential. Most people with the condition can actively participate in the community. This includes activities at schools, jobs, and various leisure activities. Some people with Down syndrome live with family, some live with friends, and some live independently.
Some newborns may need surgery to repair serious medical problems, like heart defects.
Infants with Down syndrome may take longer to feed. A child with Down syndrome will also start talking, playing, and performing other activities later than normal.
Learning opportunities may be increased with:
School programs designed to meet the child's special needs.Mainstreaming children into regular public school classes (with additional support as needed)—In children who have accomplished academic milestonesSpeech, physical, and occupational therapy may improve abilities. Therapy can help with speech, walking, and performing activities of daily living.
Professional support helps a family cope with caring for a child with birth defects and intellectual disability. Mental health professionals offer help with managing emotional problems.
There are no guidelines for preventing Down syndrome. If you have concerns about having a child with Down syndrome, consider getting genetic counseling before becoming pregnant.
Last reviewed September 2012 by Rimas Lukas, MD
Please be aware that this information is provided to supplement the care provided by your physician. It is neither intended nor implied to be a substitute for professional medical advice. CALL YOUR HEALTHCARE PROVIDER IMMEDIATELY IF YOU THINK YOU MAY HAVE A MEDICAL EMERGENCY. Always seek the advice of your physician or other qualified health provider prior to starting any new treatment or with any questions you may have regarding a medical condition.
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