Geneaura - Prenatal

Prenatal/ Fetal Genomics

Prenatal genetic counseling is a specialized service offered at GeneAura to support expectant parents in understanding the genetic aspects of pregnancy, making informed decisions about prenatal screening and testing, and preparing for the health and well-being of their unborn child. Our experienced genetic counselors provide compassionate guidance and personalized support to individuals and couples navigating the complexities of prenatal genetics.

Importance of Prenatal Screening:

Prenatal screening plays a crucial role in identifying genetic abnormalities and chromosomal disorders in the fetus, allowing for early detection, informed decision-making, and appropriate medical management. By assessing the risk of genetic conditions during pregnancy, prenatal screening empowers parents to make informed choices about their pregnancy care, including additional diagnostic testing, pregnancy management, and potential treatment options.

When to See a Genetic Counselor:

We recommend scheduling a genetic counseling appointment if you have any of the following concerns or risk factors:

➔ Advanced maternal/ paternal age (35 years or older)

➔ Personal or family history of genetic disorders or birth defects

➔ Previous pregnancy with a chromosomal abnormality or genetic condition

➔ Abnormal ultrasound findings or other fetal abnormalities detected during pregnancy

➔ Exposure to environmental or teratogenic factors that may increase the risk of birth defects

➔ Concerns about genetic screening or testing options and their implications for your pregnancy and family.

Our genetic counselors will work with you to assess your individual risk factors and provide personalized recommendations for prenatal screening and testing based on your specific needs and circumstances.

Non-Invasive Prenatal Testing (NIPT)

A simple blood test that analyzes cell-free fetal DNA in the mother's bloodstream to screen for
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First-Trimester Combined Screening

A combination of maternal blood tests and ultrasound measurements performed between
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Integrated Screening

A combination of maternal blood tests and ultrasound measurements performed between
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Diagnostic Testing

Invasive procedures such as chorionic villus sampling (CVS) and amniocentesis, which can
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The following prenatal screening tests are typically recommended during pregnancy:

First-Trimester Combined Screening: Between 11 and 14 weeks of pregnancy.

Non-Invasive Prenatal Testing (NIPT): Anytime after 10 weeks of pregnancy.

Second-Trimester Maternal Serum Screening: Between 15 and 20 weeks of pregnancy.

Fetal Anatomy Ultrasound: Between 18 and 22 weeks of pregnancy to assess fetal development and detect structural abnormalities.

Additional Diagnostic Testing (if indicated): Chorionic villus sampling (CVS) between 10 and 13 weeks of pregnancy or amniocentesis between 15 and 20 weeks of pregnancy.

At GeneAura, our dedicated team of genetic counselors provide you with the information, support, and guidance you need to make informed decisions about your pregnancy and genetic health.

We understand that navigating pregnancy can be overwhelming, and we are committed to supporting you every step of the way. Contact us today to schedule a genetic counseling appointment and take proactive steps towards a healthy and informed pregnancy.