| General
Illness Information |
 Medical
Term: |
 Down
Syndrome |
|
Common
Name: |
None Specified |
| Description: |
Down syndrome (Trisomy 21 ) is due to a
chromosomal abnormality that
is associated with mental retardation of varying degrees and may be
associated with abnormalities in many organs. Down Syndrome is
usually diagnosed at birth on the basis of typical facial
features.
The
syndrome occurs in all races with equal frequency. Incidence is 1 in
1000 births but risk varies a great deal with mothers age. More than
20% of infants with Down syndrome are born to mothers over 35 years
of age, yet older mothers bear only 7 to 8 percent of all
children..
Most
cases are identified at birth.
|
| Causes: |
Cause unknown, but usually genetic.
Down syndrome is a result of a chromosomal abnormality. In 90% of
the cases it is due to an extra chromosome 21. This means that there
are three chromosomes of the same kind (called
Trisomy) instead of the normal two of a
kind. Other chromosomal abnormalities account for the rest of the
cases of Down syndrome. In 1/3
of cases, the extra chromosome comes from the father.
|
| Prevention: |
|
Obtain genetic counseling
before starting a family-if there is a family history of Down
Syndrome in either of the partners. |
|
If over 35 years of age or
with positive family history of Down Syndrome, request blood
test (called Triple maternal Screen) which detects a certain
protein called alpha- fetoprotein in mothers blood. This test
is to be performed at 16-18 weeks pregnancy . Low levels
of alpha-fetprotein indicate an increased risk of Down
syndrome in the fetus: and in such cases, amniocentesis
should be performed.
Blood test is a very sensitive
test and therefore, it frequently gives false positive
readings. Amniocentesis is a more accurate test for detecting
Down Syndrome in the fetus. |
|
| Signs
& Symptoms |
|
|
| Risk
Factors |
|
|
| Diagnosis & Treatment |
The
diagnosis of Down syndrome can often be made before birth by
doing the screening test- Triple maternal screening test (as
mentioned under Prevention). This test is generally
recommended in pregnant women over 35 years of age.
Additionally, ultrasound scanning may help identify
physical abnormalities in the fetus at 16 to 18 weeks
gestation. After birth, diagnosis may be made from the
physical characteristics. Diagnosis can be confirmed by
testing infants blood for Trisomy 21.
|
| General
Measures: |
 |
Learn
all you can about programs and resources in your community to
help children with Down Syndrome. |
 |
Psychotherapy
or counseling for the parents. Many parents blame themselves
and need help to cope with unnecessary, harmful
guilt. |
 |
Infant
stimulation programs recommended. |
 |
Surgery
to correct congenital heart or intestinal
disorders. |
 |
Nursing
home or group-home care, if home care is not
feasible. | |
| Medications: |
 |
|
Antibiotics for
frequent, complicating infections. There is no
medication to cure Down Syndrome.
| | |
| Activity: |
|
Encourage the child to
be as active as possible (unless heart disease is
present) in a protected environment.
| | |
| Diet: |
 |
No
special diet. Extra patience may be necessary in feeding an
infant with Down Syndrome. Some have difficulty sucking or are
not eager to eat. | |
| Possible
Complications : |
 |
Increased
susceptibility to leukemia and thyroid disease. |
 |
Increased
susceptibility to infections. Recurrent ear infection makes
them prone to hearing problems. |
 |
Congestive
heart failure caused by congenital heart
abnormalities. |
 |
Alzheimer's
disease in 1/3 of patients over age 40. |
 |
Vision problems because of changes
in the corneas and lenses. | |
| Prognosis |
| Special
education and training allow many children with Down Syndrome
to lead happy, loving and useful lives. Life expectancy is
reduced. Few persons with Down Syndrome reach age
40. | |
| Other |
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