Dealing With Down Syndrome
Down syndrome is a genetic disorder caused by abnormal cell division. The result is an extra copy of chromosome 21. This extra copy of genetic material is the cause of the physical characteristics of a person with Down syndrome and the reason why there may be some developmental difference in a patient who has this extra chromosome.What is Down Syndrome and What is the Cause?
Patients with an entire extra copy of chromosome 21 have Down syndrome. The most common identification of people with Down syndrome is their face typically looks a bit different. Their eyes often have more slanted folds of skin at the inner corners. They typically have a smaller and flatter head, flatter ears, a large, thick tongue, and a shorter neck. People with Down syndrome also tend to be shorter. Other physical symptoms include poor muscle tone; hyper flexibility; short, broad hands with a single crease across the hands, broad feet with short toes and a small oral cavity or enlarged tongue.
Down syndrome is caused by a random type of error in the process of cell division which ends up leaving a duplicate copy of chromosome 21. This particularly type of cell division error is called nondisjunction. Normally when a cell divides, the chromosome pairs split off and each new cell gets one each. When nondisjunction occurs, however, the cell divides but some chromosomes do not split off. One new cell ends up with duplicate chromosomes and the other has none at all. Nondisjunction occurs during the formation of an egg or sperm and appears to be a totally random occurrence. Research has not been able to link any environmental or other factors to an increased risk of nondisjunction.Are There Different Types of Down Syndrome?
There are three major types of Down syndrome. Trisomy 21 is a chromosomal condition that occurs when there are three copies of a particular chromosome instead of the normal two copies. Trisomy 21 is caused by the presence that extra chromosome. This happens as a result of an anomaly in cell division during development of either the egg or sperm during conception. It is the most severe form of Down but there are many Trisomy 21 children who go on to live healthy, happy, and productive lives. Trisomy 21 makes up an estimated 95% of those who have Down syndrome cases. Not that it matters but 88% of these cases stem from non-disjunction of the mother's egg cell.
The second type of is called translocation which accounts for 4% of Down syndrome cases. This is the result of the extra chromosome 21 breaking off and becoming attached or translocated to another chromosome. The presence of this extra piece of chromosome 21 cause some Down syndrome characteristics. As you might expect, the signs and symptoms in a patient with translocation are much less severe and may not be identifiable with the naked eye. Patients with translocation may have an increased risk of a child with Down syndrome.
The third type of Down syndrome is called mosaicism, where the extra chromosome 21 is present in some, but not all cells. Mosaicism accounts for only one percent of all Down syndrome cases. This rare type of Down is also the least severe. Research indicates that individuals with mosaic Down syndrome may have fewer characteristics of Down syndrome than those with other types of Down syndrome.Is There a way to Test for Down syndrome?
There is a test for Down syndrome. The most common test is amniotic fluid sampling by amniocentesis or obtaining tissue by chorionic villus sampling ("CVS"). But CVS is invasive and carries risks to the mother and what might be a very healthy fetus. CVS can cause a miscarriage. It may also cause fetal limb defects. The new MaterniT21 blood test is non-evasive and can catch 98% of fetuses that have Down syndrome. The test can cost a few hundred dollars even for patients who do have health insurance (the price has come down).What is Life Like With Down Syndrome?
It is true that people with Down syndrome often have physical and intellectual development that is less advanced than their peers. But the good news is that many people with most people with Down syndrome are happy, productive people who have relatively medically uneventful lives. It is not fair to say Down patients suffer no more illness than their peers with normal chromosomes. But for many, the problems are navigable. Technology and research for Down syndrome have yielded great results. Even those with birth defects often have normal life spans. This is because advances in pediatric and cardiothoracic surgery have allowed surgical solutions to gastrointestinal and cardiac anomalies. For a minority of Down syndrome patients, there is a malady of potential complicationsIs Down Syndrome Inherited From the Mother or Father?
Parents are eager to blame themselves when their child has Down syndrome But there is no evidence that there environmental factors or something the parents did before or after childbirth that cause this condition. Which parent gave the child the extra chromosome? It could be either the mother or the father (and it does not matter). But it is not a genetic thing that is inherited. It is just a random thing that happened during cell division early in the pregnancy.Down Syndrome Bad Statistics and Facts
There are some of the less encouraging facts about Down syndrome:
- 90 percent suffer from periodontal disease
- 70 percent suffer an astigmatism
- 60 to 80 percent have hearing deficits.
- 0-70 percent suffer vision and hearing deficits
- 40-45 percent suffer from congenital heart disease (death in infancy accounts for one-third of patients
- 30 percent suffer from sleep apnea
- 25 percent over the age of 35 will develop the clinical signs and symptoms of Alzheimer's-type dementia
- 25-40 percent of Down syndrome patients suffer hypothyroidism
- 15 percent suffer from thyroid disease.
- 5 to 10 percent of people with Down syndrome suffer from seizure disorders.
- Acute leukemia occurs with an increased frequency (still less than 1%)
- Greater risk for thyroid dysfunction, kneecap subluxation, hip dislocation, celiac disease, Hirschsprung disease, autoimmune disease, intestinal abnormalities, cataracts, atlantoaxial instability, Alzheimer's disease, epilepsy, and infection.
The risk of cell division errors like nondisjunction increases as eggs get older, so as women age their chances of having a baby with Down syndrome increase. Statistics show that the chances of having a baby spike dramatically when the mother is 35 years or older.Is There an Advocacy Group for People With Down Syndrome?
The National Down Syndrome Congress, founded in 1974, is the national advocacy organization of families of children with Down syndrome, and of professionals and interested other persons who provide services to or otherwise assist persons with Down syndrome. Through over 500 local parent support groups, the NDSC carries on a broad range of activities. They fight to protect and secure the rights of persons with Down syndrome, the provision of information and other assistance to families of persons with Down syndrome to help them meet the special needs of these individuals, and the promotion of public understanding of persons with Down syndrome.
Additional Literature and Resources
- Mitchell RB, Call E, Kelly J.: Ear, Nose and Throat Disorders in Children with Down Syndrom. 2003 113(2):259-63.
- Heller JH, Spiridigliozzi GA, et al: Clinical Trials in Children with Down Syndrome: Issues from a Cognitive Research Perspective. Am J Med Genet C Semin Med Genet. 2006 Aug 15; 142C(3) : 187-95.
- Vintzileos AM, et al., Cost-Benefit Analysis of Prenatal Diagnosis for Down Syndrome Using the British or the American Approach, Obstetrics and Gynecology 2000; 95(4): 577-583.
- Haddow JE, et al. Prenatal Screening for Down's Syndrome with Use of Maternal Serum Markers. N Engl J Med 1992;327:588-93.
- Shott, S. R., Joseph, A., Heithaus, D.: Hearing Loss in Children with Down Syndrome. International Journal of Pediatric Otorhinolaryngology, 2001: 61: 199-205.
- Lott IT: Down syndrome, aging and Alzheimer's disease: A clinical review. Annals NY Acad Sci. 1982;396:15-27 (related article by Lott in 2001)