4.2 Chromosomal Abnormalities and Genetic Testing
Learning Objectives
- Describe chromosomal abnormalities
- Explain the types of prenatal testing
Chromosomal Abnormalities
A chromosomal abnormality occurs when a child inherits too many or too few chromosomes. The most common cause of chromosomal abnormalities is the age of the parent providing the eggs. A 20-year-old gestational parent has a 1 in 800 chance of having a child with a common chromosomal abnormality. A gestational parent of 44, however, has a one in 16 chance. It is believed that the problem occurs when the ovum is ripening prior to ovulation each month. As the gestational parent ages, the ovum is more likely to suffer abnormalities at this time.
Another common cause of chromosomal abnormalities occurs because the gametes do not divide evenly when they are forming. Therefore, some cells have more than 46 chromosomes. In fact, it is believed that close to half of all zygotes have an odd number of chromosomes. Most of these zygotes fail to develop and are spontaneously aborted by the body. If the abnormal number occurs on pair # 21 or # 23, however, the individual may have certain physical or other abnormalities.
One of the most common chromosomal abnormalities is on pair # 21. Trisomy 21 occurs when there are three rather than two chromosomes on #21. A person with Down syndrome has distinct facial features, intellectual development disorder (intellectual disability), and oftentimes heart and gastrointestinal disorders. Symptoms vary from person to person and can range from mild to severe. With early intervention, the life expectancy of persons with Down syndrome has increased in recent years. Keep in mind that there is as much variation in people with Down Syndrome as in most populations and those differences need to be recognized and appreciated.
Watch It
Watch the following video clip about Down Syndrome from the National Down Syndrome Society:
You can view the transcript for “Down Syndrome – Ability Awareness PSA Video” here (opens in new window).
Prenatal Testing
Prenatal testing consists of prenatal screening and prenatal diagnosis, which are aspects of prenatal care that focus on detecting problems with the pregnancy as early as possible. These may be anatomic and physiologic problems with the health of the zygote, embryo, or fetus, either before gestation even starts or as early in gestation as practical. Prenatal screening focuses on finding problems among a large population with affordable and noninvasive methods. The most common screening procedures are routine ultrasounds, blood tests, and blood pressure measurement. Prenatal diagnosis focuses on pursuing additional detailed information once a particular problem has been found, and can sometimes be more invasive.
Screening can detect problems such as neural tube defects, anatomical defects, chromosome abnormalities, and gene mutations that would lead to genetic disorders and birth defects, such as spina bifida, cleft palate, Downs Syndrome, Tay–Sachs disease, sickle cell anemia, thalassemia, cystic fibrosis, muscular dystrophy, and fragile X syndrome. Some tests are designed to discover problems which primarily affect the health of the gestational parent, such as PAPP-A to detect pre-eclampsia or glucose tolerance tests to diagnose gestational diabetes. Screening can also detect anatomical defects such as hydrocephalus, anencephaly, heart defects, and amniotic band syndrome.
Common prenatal diagnosis procedures include amniocentesis and chorionic villus sampling. Because of the miscarriage and fetal damage risks associated with amniocentesis and CVS procedures, many gestational parents prefer to first undergo screening so they can find out if the fetus’ risk of birth defects is high enough to justify the risks of invasive testing. Screening tests yield a risk score which represents the chance that the baby has the birth defect; the most common threshold for high-risk is 1:270. A risk score of 1:300 would, therefore, be considered low-risk by many physicians. However, the trade-off between the risk of birth defects and risk of complications from invasive testing is relative and subjective; some parents may decide that even a 1:1000 risk of birth defects warrants an invasive test while others wouldn’t opt for an invasive test even if they had a 1:10 risk score.
The American College of Obstetricians and Gynecologists (ACOG) guidelines currently recommend that all gestational parents, regardless of age, be offered invasive testing to obtain a definitive diagnosis of certain birth defects. Therefore, most physicians offer diagnostic testing to all their patients, with or without prior screening and let the patient decide.
Watch It
Watch this video to learn more about prenatal testing and screening during pregnancy.
You can view the transcript for “Screening in Pregnancy” here (opens in new window).
Try It
Licenses & Attributions (Click to expand)
CC LICENSED CONTENT, SHARED PREVIOUSLY
- Chromosomal Abnormalities and Genetic Testing. Provided by: Lumen Learning. Located at: https://courses.lumenlearning.com/wm-lifespandevelopment/chapter/chromosomal-abnormalities-and-genetic-testing/. License: CC BY: Attribution
- Psyc 200 Lifespan Psychology. Authored by: Laura Overstreet. Located at: http://opencourselibrary.org/econ-201/. License: CC BY: Attribution
- Chromosome abnormality. Provided by: Wikipedia. Located at: https://en.wikipedia.org/wiki/Chromosome_abnormality. License: CC BY-SA: Attribution-ShareAlike
ALL RIGHTS RESERVED CONTENT
- Down Syndrome – Ability Awareness PSA Video. Authored by: rosaryfilms. Located at: https://www.youtube.com/watch?v=TIcbFrt4F_c. License: Other. License Terms: Standard YouTube License
- Screening in Pregnancy. Authored by: Michigan Medicine. Located at: https://www.youtube.com/watch?v=odYHHgzsc_4. License: Other. License Terms: Standard YouTube License