Antenatal and prenatal refer to the time period before birth, during pregnancy. The care that you receive from your obstetrician while pregnant is referred to as antenatal or prenatal care. The American College of Obstetricians and Gynecologists recommends that all pregnant women see an obstetrician for prenatal care

Regular appointments with an obstetrician, in conjunction with prenatal tests, can help mothers avoid potential complications during pregnancy. During these appointments, a doctor will perform routine prenatal tests, like ultrasound scans and blood tests, to monitor the health of the mother. In addition, optional prenatal tests and screenings that assess the health of the baby are available. These testing options are discussed in further detail below.

Antenatal Testing and Inherited Genetic Conditions

Genetic carrier screening is an antenatal test that can be performed before pregnancy. This test is centered around understanding an individual’s or a couple’s risk of having a child with a certain genetic condition. Genetic carrier screening is recommended for individuals and couples who have a history of an inherited genetic condition, like cystic fibrosis (a disorder affecting the lungs that a child may develop when both parents carry the gene or it). This test can be performed before or during pregnancy.

Individuals who have a family history of an inherited disorder are at risk of being genetic carriers. A genetic carrier is a person who has inherited, or received, a mutated copy of a gene but does not show signs or symptoms of a genetic disorder. However, if two copies of this mutated gene are inherited, the condition will develop. Carriers are at risk of passing on the mutated gene to their children.

If both partners in an expecting couple test positive as genetic carriers for the same disorder, they will be offered the option of additional diagnostic testing later on in the pregnancy.

Diagnostic Antenatal Tests

Antenatal diagnostic tests involve collecting a sample of tissue from the baby’s environment in order to test the child’s DNA for genetic mutations associated with inherited disorders. Antenatal diagnostic tests include:

  • Amniocentesis: Amniocentesis is performed between the 15th and 20th week of the pregnancy. During this procedure, a sample of amniotic fluid is collected and analyzed in a laboratory to detect genetic or chromosomal abnormalities in the baby.
  • Chorionic villus sampling (CVS): CVS is performed between the 10th and 13th week of the pregnancy. During this procedure, a sample of tissue from the placenta is collected and analyzed in a laboratory to detect genetic or chromosomal abnormalities in the baby.

If you’d like more information regarding the timing of prenatal testing, the American College of Obstetricians and Gynecologists provides a prenatal testing timeline on their website.

Consider Working with a Genetic Counselor

Genetic counselors are trained professionals who guide individuals and couples through the antenatal testing process. Working with a genetic counselor can help ensure that the information received by potential mothers is accurate, and that there is a point of reference from which to make informed decisions regarding pregnancy.

SOURCES:

https://www.pregnancybirthbaby.org.au/routine-antenatal-tests

https://www.acog.org/Patients/FAQs/Good-Health-Before-Pregnancy-Preconception-Care

https://www.acog.org/Patients/FAQs/Reducing-Risks-of-Birth-Defects#pregnancy

https://www.mayoclinic.org/diseases-conditions/cystic-fibrosis/symptoms-causes/syc-20353700

http://www.healthofchildren.com/A/Antenatal-Testing.html

https://www.acog.org/Clinical-Guidance-and-Publications/Committee-Opinions/Committee-on-Obstetric-Practice/Group-Prenatal-Care