DOWN SYNDROMEYour Guide To Better Understanding The Journey Of Your Consumers With Down Syndrome

WHAT IS DOWN SYNDROME? Down syndrome is a genetic disorder that causes lifelong

mental retardation, developmental delays and other problems. Down syndrome varies in severity, so developmental problems range from moderate to serious.

Down syndrome is the most common genetic cause of severe learning disabilities in children, occurring in one in every 700 to 800 infants.

Increased understanding of Down syndrome and early interventions make a big difference in the lives of both children and adults with Down syndrome.

There's no way to prevent Down syndrome. However, if one is at high risk of having a child with Down syndrome or has already had one child with Down syndrome, they may wish to consult a genetic counselor before becoming pregnant.

A genetic counselor estimate their chances of having a child with Down syndrome. He or she can also explain the prenatal tests that will be offered and help figure out the pros and cons of testing.

COMMON SYMPTOMSChildren with Down syndrome have a distinct facial appearance.

Though not all children with Down syndrome have the same features, some of the more common features are:

Flattened facial features Protruding tongue Small head Upward slanting eyes, unusual for the child's ethnic group Unusually shaped ears Children with Down syndrome may also have: Poor muscle tone Broad, short hands with a single crease in the palm Relatively short fingers Excessive flexibility Infants born with Down syndrome may be of average size, but

typically they grow slowly and remain shorter than other children of similar age. Children with Down syndrome also have some degree of mental retardation, most often in the moderate range.

CAUSES The cause of Down syndrome is one of three types of abnormal cell

division involving chromosome 21. All three abnormalities result in extra genetic material from chromosome 21, which is responsible for the characteristic features and developmental problems of Down syndrome. The three genetic variations that can cause Down syndrome include:

Trisomy 21. More than 90 percent of cases of Down syndrome are caused by trisomy 21. A child with trisomy 21 has three copies of chromosome 21 — instead of the usual two copies — in all of his or her cells. This form of Down syndrome is caused by abnormal cell division during the development of the sperm cell or the egg cell.

Mosaic Down syndrome. In this rare form of Down syndrome, children have some cells with an extra copy of chromosome 21. This mosaic of normal and abnormal cells is caused by abnormal cell division after fertilization.

Translocation Down syndrome. Down syndrome can also occur when part of chromosome 21 becomes attached (translocated) onto another chromosome, before or at conception. Children with translocation Down syndrome have the usual two copies of chromosome 21, but they also have additional material from chromosome 21 stuck to the translocated chromosome. This form of Down syndrome is uncommon.

There are no known behavioral or environmental factors that cause Down syndrome.

CAUSES CONT’D Is it inherited?

Most cases of Down syndrome aren't inherited. They're caused by a mistake in cell division during the development of the egg, sperm or embryo.

Translocation Down syndrome is the only form of the disorder that can be passed from parent to child. However, only about 4 percent of children with Down syndrome have translocation. And only about half of these cases are inherited from one of the parents.

In these translocation cases, the mother or father is a balanced carrier of the translocation, which means he or she has some rearranged genetic material, but no extra genetic material. A balanced carrier has no signs or symptoms of Down syndrome, but he or she can pass the translocation on to children.

The chance of passing on the translocation depends on the sex of the parent who carries the rearranged chromosome 21:

If the father is the carrier, the risk is about 3 percent. If the mother is the carrier, the risk is about 12 percent.

RISK FACTORSSome parents have a greater risk of having a baby with

Down syndrome. Risk factors include: Advancing maternal age. A woman's chances of

giving birth to a child with Down syndrome increase with age because older eggs have a greater risk of improper chromosome division. By age 35, a woman's risk of conceiving a child with Down syndrome is 1 in 400. By age 45, the risk is 1 in 35. However, most children with Down syndrome are actually born to women under age 35 because younger women have far more babies.

Having had one child with Down syndrome. Typically, a woman who has one child with Down syndrome has about a 1 percent chance of having another child with Down syndrome.

Being carriers of the genetic translocation for Down syndrome. Both men and women can pass the genetic translocation for Down syndrome on to their children.

COMPLICATIONS Heart defects. Approximately half the children with Down syndrome are

born with some type of heart defect. These heart problems can be life-threatening and may require surgery in early infancy.

Leukemia. Young children with Down syndrome are more likely to develop leukemia than are other children.

Infectious diseases. Because of abnormalities in their immune systems, those with Down syndrome are much more susceptible to infectious diseases, such as pneumonia.

Dementia. Later in life, people with Down syndrome have a greatly increased risk of dementia. Signs and symptoms of dementia often appear before age 40 in people with Down syndrome.

Sleep apnea. Because of soft tissue and skeletal alterations that lead to the obstruction of their airways, children with Down syndrome are at greater risk of obstructive sleep apnea.

Obesity. People with Down syndrome have a greater tendency to be obese than does the general population.

Other problems. Down syndrome may also be associated with other health conditions, including gastrointestinal blockage, thyroid problems, hearing loss, skeletal problems and poor vision.

Life expectancy Life spans have increased dramatically for people with Down syndrome. In 1929, a baby born with Down syndrome often didn't live to age 10. Today, someone with Down syndrome can expect to live to 50 and beyond, depending on the severity of his or her health problems. Life span continues to increase because of early interventions and better care.

TESTS AND DIAGNOSIS Screening tests during pregnancy

Various screening tests can help identify whether there is high risk of carrying a baby with Down syndrome. Blood tests typically have been offered around the 16th week of pregnancy to screen for Down syndrome, spina bifida and various other chromosomal disorders.

For an earlier risk assessment, the first trimester combined test, done in two steps from the week 11 to week 13 of pregnancy, may be the best choice. About 5 percent of women who undergo the first trimester combined test have a false-positive result, meaning they're identified incorrectly as having a high risk of delivering a baby with Down syndrome. The first trimester combined test includes:

Ultrasound. The doctor uses ultrasound to measure a specific region on the back of a baby's neck. This is known as a nuchal translucency screening test. When abnormalities are present, more fluid than usual tends to collect in this tissue.

Blood tests. Results of the ultrasound are paired with blood tests that measure levels of pregnancy-associated plasma protein-A (PAPP-A) and a hormone known as human chorionic gonadotropin (HCG). Abnormal levels of PAPP-A and HCG may indicate a problem with the baby.

TESTS AND DIAGNOSIS CONT’D If early assessment isn't the first priority, you can have full

integrated testing, which is done in two parts during the first two trimesters of your pregnancy. The results of the two parts are combined to estimate your risk that the baby has Down syndrome. Only about 1 percent of women have a false-positive result with full integrated testing, so fewer women require more invasive testing.

First trimester. Part one includes an ultrasound to measure nuchal translucency and a blood test to measure PAPP-A.

Second trimester. Done at 15 to 20 weeks of pregnancy, the quad screen measures the blood level of four pregnancy-associated substances, alpha-fetoprotein, estriol, HCG, and inhibin A.

If a screening test indicates a high risk of Down syndrome, a more invasive test may be used to determine whether the baby actually has Down syndrome.

About one in 20 women will have a positive result with any of these screening tests — far more than those who eventually deliver a baby with a chromosomal abnormality. In fact, most women who have a positive result from a screening test deliver healthy babies.

TESTS AND DIAGNOSIS CONT’DDiagnostic tests during pregnancy

If the screening tests are positive or worrisome or if at high risk of having a baby with Down syndrome, further testing to confirm the diagnosis may be necessary. Diagnostic tests that can identify Down syndrome include:

Amniocentesis. A sample of the amniotic fluid surrounding the fetus is withdrawn through a needle inserted into the mother's uterus. This sample is then used to analyze the chromosomes of the fetus. Doctors usually perform this test after 15 weeks of gestation. The test carries a one in 200 risk of miscarriage.

Chorionic villus sampling (CVS). Cells taken from the mother's placenta can be used to analyze the fetal chromosomes. Typically performed between the ninth and 14th week of pregnancy, this test carries a one in 100 risk of miscarriage.

Percutaneous umbilical blood sampling (PUBS). Blood is taken from a vein in the umbilical cord and examined for chromosomal defects. Doctors generally perform this test after 18 weeks of gestation. This test carries a greater risk of miscarriage than does amniocentesis or chorionic villus sampling. Generally, this test is only done when speed of diagnosis is essential.

Each of these three tests is 98 to 99 percent accurate in diagnosing Down syndrome before birth.

Diagnostic tests for newbornsAfter birth, the initial diagnosis of Down syndrome is often based on the baby's appearance. If your child displays some or all of the characteristics of Down syndrome, your doctor probably will order a test called a chromosomal karyotype. This test is an analysis of your child's chromosomes. If there's an extra chromosome 21 present in all or some of the cells, the diagnosis is Down syndrome.

TREATMENTS AND DRUGS Early intervention programs

Ask a doctor about early intervention programs in the area. These specialized programs — in which children with Down syndrome are stimulated at an early age with appropriate sensory, motor and cognitive activities — are available in most states.

Programs vary from location to location, but they usually involve therapists and special educators whose goal is to help your baby develop motor skills, language, social skills and self-help skills.

Developing a team If the child has Down syndrome, you'll likely build a team of specialists that, depending on the child's particular needs, will provide the child's medical care and help him or her develop skills as fully as possible. In addition to your primary care pediatrician, your team may include:

A pediatric cardiologist A pediatric gastroenterologist A pediatric endocrinologist A developmental pediatrician An audiologist A physical therapist A speech pathologist An occupational therapist What to expect

In general, children with Down syndrome usually meet developmental milestones, but it may take them longer than it does a child without Down syndrome. For example, children with Down syndrome may take twice as long to sit, crawl, walk or talk. However, early intervention programs, started as soon as possible, may give kids with Down syndrome the best chance of success.

SOURCE OF INFORMATION

http://www.mayoclinic.com/health/down-syndrome/DS00182