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Clinical Genomics LaboratoryFor additional uptodate testing information and our most current requisitions, please visit our website: http://www.iwk.nshealth.ca/clinicalgenomics/5850/5980 University
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How to fill out fetal genetic testing

01
Consult with healthcare provider to determine if fetal genetic testing is recommended.
02
Schedule an appointment for the test.
03
Follow any preparation instructions provided by healthcare provider.
04
Provide a sample of blood or tissue, typically through a blood draw or amniocentesis procedure.
05
Wait for results to be analyzed and communicated by healthcare provider.

Who needs fetal genetic testing?

01
Fetal genetic testing is recommended for pregnant women who are at higher risk for having a baby with genetic abnormalities, such as women over the age of 35, women with a family history of genetic disorders, or couples with a previous child with a genetic condition.
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Fetal genetic testing is a medical procedure that analyzes the genetic material of a fetus to identify genetic disorders and conditions, typically performed during pregnancy.
Healthcare providers who perform fetal genetic testing are required to file the necessary documentation, typically along with the expecting parents' consent.
To fill out fetal genetic testing, healthcare providers must complete specific forms that include patient information, test type, and consent, ensuring all details are accurate before submission.
The purpose of fetal genetic testing is to screen for genetic abnormalities or conditions in the fetus, allowing for informed decision-making by parents and healthcare providers.
The information reported on fetal genetic testing usually includes patient demographics, test results, type of genetic test performed, and any relevant medical history.
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