Many
women today are waiting until later in life to have children. In the United
States, birth rates for women in their 30s are at the highest levels in three
decades. However, an older mother may be at increased risk for miscarriage,
birth defects, and pregnancy complications such as twins, high blood pressure,
gestational diabetes, and difficult labors. Some studies show that while there
may be a greater likelihood of pregnancy complications in older women, their
babies may not have more problems than babies of younger women. This is more
likely when women receive prenatal care and give birth in a healthcare facility
equipped to care for high-risk mothers and babies.
Risks for Chromosome
Abnormalities by Maternal Age
Maternal
Age
|
Down
syndrome
|
Any
abnormality
|
15
to 24 years
|
1/1300
|
1/500
|
25
to 29 years
|
1/1100
|
1/385
|
35
years
|
1/350
|
1/178
|
40
years
|
1/100
|
1/63
|
45
years
|
1/25
|
1/18
|
It
is possible that risks may be higher as many statistics only report live births
and do not take into account pregnancies with chromosomal abnormalities that
were terminated or ended due to natural pregnancy loss. There are approximately
400 different types of chromosome abnormalities that have been observed in
humans, however, many are rare. The risk for Down syndrome makes up almost half
of the maternal age risk for chromosome abnormalities.
In general, for women under the age of 40,
after having one child with Down syndrome, the chance of having another baby
with Down syndrome is 1 percent. After age 40, the recurrence risk for Down
syndrome is based on the age of the mother at delivery. It is important to know
that about 75 percent of babies with Down syndrome are born to women under the
age of 35. This is because women under the age of 35 have more babies than
women over 35. The physician may refer parents to a genetic specialist or
genetic counselor who can explain the results of chromosomal tests in detail,
including what the recurrence risks may be in another pregnancy and what tests
are available to diagnose chromosome problems before a baby is born.
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