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Conditions Screened

Prenatal screening provides a pregnant person with their individual risk of having a child with a chromosome difference. It does not screen for all chromosome abnormalities, so some may be missed.
Some of the common conditions that prenatal screening will test for are:

Down syndrome

Babies and children with Down syndrome are individuals who are just as unique and highly variable as anyone else.  An individual with Down syndrome has an extra copy of chromosome 21 (trisomy 21).  This usually causes mild to moderate intellectual disability, which means that adults will typically function at the level of an 8-10 year old.  An individual with Down syndrome is expected to learn to read and write and to be physically active, however major developmental milestones will be delayed.  Individuals with Down syndrome have a greater possibility of health conditions than the average person, such as heart, stomach, bowel, thyroid, vision and hearing problems.  Treatment is available for many of these conditions. There is no way to predict how serious or mild these differences will be. People with Down syndrome generally live into their fifties. In general, about one in 1000 babies born has Down syndrome. The chance of having a child with Down syndrome increases with the pregnant person/egg donor’s (in the case of a donated egg) age (See Table below for specific information).  For more information on Down syndrome, visit the Canadian Down Syndrome Society website.

Trisomy 18 (Edward syndrome)

Babies with trisomy 18 have an extra chromosome 18. Every individual with trisomy 18 is different, however serious intellectual disabilities and congenital anomalies that may affect many organ systems (e.g. heart, kidneys) are expected. Many pregnancies with trisomy 18 will miscarry.  Most babies born with trisomy 18 do not survive past the first few months of life.  About 10% of infants will survive up to 5 years of age, or occasionally longer. Long-term survivors are described as socially interactive with significant physical and intellectual disabilities (e.g. having few words).  In general, about one in 6,000 babies born has trisomy 18. The chance of having a child with trisomy 18 increases with the pregnant person/egg donor’s age.  For more on trisomy 18, visit The Trisomy 18 Foundation website.

Open Neural Tube Defects

The neural tube is a structure in the early development of the central nervous system (the spinal cord and the brain). This structure is completely formed by about 6 weeks of pregnancy. Incomplete or failed formation of the neural tube leads to congenital anomalies of the brain or spinal cord and nerves. The effects of a neural tube defect are extremely varied and depend on the location and size of the defect. Open neural tube defects are the most common and serious.  The neural tube defect is closed if the defect is covered by skin and the neural tissue is not exposed to amniotic fluid.  A neural tube defect involving the spinal cord is called spina bifida. Spina bifida causes physical disabilities such as difficulty walking, and controlling the bladder and/or bowel. People with spina bifida may also have intellectual disabilities. Treatment can help with many of the physical disabilities. A neural tube defect involving the brain is called anencephaly.  A baby with anencephaly will be stillborn or die shortly after birth. In Canada, the chance of having a baby with an open neural tube defect is about one in 1000 live births. The chance does not increase with the pregnant person/egg donor’s age.  The chance does decrease when a prenatal vitamin with folic acid is taken.  For more on spina bifida, see the Spina Bifida & Hydrocephalus Association of Ontario website.  Talk to your health care provider about folic acid and prenatal vitamins.

Additional conditions which may be screened for by prenatal screening:

Trisomy 13 (Patau syndrome)

Babies with trisomy 13 have an extra chromosome 13. In general between 1/8,000 and 1/15,000 of babies born has trisomy 13. The chance of having a child with trisomy 13 increases with a pregnant person/egg donor’s age. Every individual with trisomy 13 is different; however each individual is expected to have both serious intellectual disabilities and congenital anomalies, including differences of the brain, heart, eyes and face.  Most pregnancies with trisomy 13 will miscarry.  About 5-10% of infants will survive the first year of life.  There are some individuals who have lived to adulthood. For information on trisomy 13, visit Support Organization for Trisomy 18, 13 and Related Disorders (SOFT) website.

Sex chromosome differences

Typically, each mature human cell contains 23 chromosome pairs (46 chromosomes in total).  One of these chromosome pairs, the 23rd pair, is the sex chromosomes.  A female cell will usually have two X chromosomes and a male cell will have one X chromosome and one Y chromosome.  Some prenatal screening and diagnostic testing can identify extra or missing X and/or Y chromosomes.  There are several disorders with sex chromosome differences.  Generally, these types of genetic differences are quite common occurring in about 1 in 500 individuals.  Expected features are variable and depend on which chromosome is extra or missing.  Some features maybe as mild as tall or short size.  There may be differences in development such as delayed speech or learning differences.  There may be associated health issues involving puberty or the heart. For a brief overview of chromosomes and some chromosome disorder visit the Genomic Resource Centre by the World Health Organization (WHO).

Risk of Chromosome Abnormalities in Liveborn Infants at Term by Pregnant Person’s Age

Each pregnant person starts with an a priori risk of having a child with a chromosome abnormality based on their age at the time of delivery.  Screening adjusts this risk, either lowering or raising the risk based on the analytes measured in the blood and/or nuchal translucency measurement.

     Pregnant Person’s/      Donor’s Age (yrs)

Risk of Down Syndrome

Risk of ANY Chromosome Abnormality

20

1/1,650

1/530

21

1/1,650

1/530

22

1/1,430

1/500

23

1/1,430

1/500

24

1/1,250

1/480

25

1/1,250

1/480

26

1/1,175

1/480

27

1/1,110

1/450

28

1/1,050

1/430

29

1/1,000

1/420

30

1/950

1/390

31

1/900

1/390

32

1/770

1/320

33

1/625

1/285

34

1/500

1/240

35

1/385

1/180

36

1/300

1/150

37

1/225

1/125

38

1/175

1/100

39

1/135

1/80

40

1/100

1/65

41

1/80

1/50

42

1/60

1/40

43

1/50

1/30

44

1/40

1/25

45

1/30

1/19

46

1/23

1/15

47

1/18

1/11

48

1/14

1/9

49

1/11

1/7

Adapted from:
Hook EB, Cross PK, Schreinemachers DM,  Chromosomal abnormality rates at amniocentesis and in live-born infants. JAMA 1983; 249: 2034-38.
Hook EB. Rates of chromosomal abnormalities at different maternal ages. Obstet Gynecol 1981; 53: 282-85.