How do chromosome abnormalities happen?
Chromosome abnormalities typically occur as a result of one, or more, of the following:
Chromosome abnormalities usually happen as a result of an error in cell division. Meiosis is the name used to describe the cell division that the egg and sperm undergo when they are developing. Normally, meiosis causes a halving of chromosome material, so that each parent gives 23 chromosomes to a pregnancy.
The result is an egg or sperm with only 23 chromosomes. When fertilization occurs, the normal 46 total number of chromosomes results in the fetus. If meiosis does not occur properly, an egg or sperm could end up with too many chromosomes, or not enough chromosomes. Upon fertilization, the baby could then receive an extra chromosome (called a trisomy), or have a missing chromosome (called a monosomy).
While pregnancies with a trisomy or a monosomy may go to full-term and result in the birth of a child with health problems, it is also possible that the pregnancy may miscarry, or that the baby is stillborn (not born alive), because of the chromosome abnormality. In studies of first trimester miscarriages, about 60 percent (or more) are chromosomally abnormal. In studies of babies who are stillborn, 5 to 10 percent have a chromosome abnormality.
Mitosis is the name used to describe the cell division that all other cells, besides the egg and sperm, undergo when they are developing. Normally, mitosis causes a duplication, followed by a halving of chromosome material, so that each cell doubles the number of chromosomes to 92, and then splits in half, so that the normal total of 46 is resumed. Mitosis begins in the fetus after fertilization.
This process repeats itself, until the entire baby is formed. Mitosis continues throughout our lifetime, to regenerate new skin cells, new blood cells, and other types of cells that are damaged or that simply die off.
During pregnancy, an error in mitosis can occur, just like the error previously described in meiosis. If the chromosomes do not split into equal halves, the new cells can have an extra chromosome (47 total) or have a missing chromosome (45 total). This is another way a baby can be born with a chromosome abnormality. Errors in mitosis are responsible for some cases of mosaicism.
When a mother will be 35 years of age at delivery (or older), she may be referred for genetic counseling or for prenatal diagnosis, such as an amniocentesis, because of her age. There is a fundamental difference in the way that eggs and sperm are made. Women are born with all the eggs they will ever have, and they begin to mature during puberty. Over time, there are fewer and fewer eggs available in the ovaries. If a woman is 35 years old, the eggs in the ovaries are also 35 years old. The risk for a baby to be born with a chromosome abnormality increases with the age of the mother. Some scientists and physicians believe that this is because the eggs are aging, and may have the incorrect number of chromosomes at the time of fertilization. Errors in meiosis may be more prone to happen as a result of the aging process.
Men, on the other hand, produce new sperm continually. Therefore, if a man is 35 years of age, his sperm are not 35 years of age. However, recent studies have shown that men over the age of 45 years may have an increased risk for new (de novo) autosomal dominant conditions in their children.
Many parents who have a child with a chromosome abnormality wonder whether the various environmental exposures they have had over the years contributed to having a baby with a chromosome abnormality. To date, there is not anything specific in the environment, such as X-rays, medications, foods, microwave ovens, etc., that has been found to be the reason for a baby to be born with a chromosome abnormality. In fact, most parents who have a child with a chromosome abnormality, when compared to those parents who do not have a child with a chromosome abnormality, have no difference in habits, lifestyles, or environmental exposures.