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Genetic Testing

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Genetic Testing in Fertility Treatment

Genetic testing plays a crucial role in modern fertility treatment, helping to identify genetic abnormalities that may affect embryo development, pregnancy outcomes, and the health of future children.

At Seeds of Innocence, we offer comprehensive genetic testing services to help couples make informed decisions about their fertility journey.

Genetic Testing

Why is Genetic Testing Done?

Genetic testing is done to identify genetic or chromosomal abnormalities that may affect fertility, pregnancy outcomes, or the health of future children.

Identify genetic causes of infertility
Screen embryos for chromosomal abnormalities (PGT)
Carrier screening for inherited conditions
Inform treatment and family planning

What Does Genetic Testing Check?

Depending on the test, genetic testing may check:

Chromosomal abnormalities (aneuploidy, structural)
Single-gene mutations
Carrier status for inherited disorders
Embryo genetic health (PGT-A, PGT-M, PGT-SR)

How is Genetic Testing Performed?

Methods vary by test type: blood/saliva for carrier or karyotype testing; embryo biopsy for PGT; amniotic fluid or CVS for prenatal testing. Our team will explain the specific steps for your test.

Sample collection (blood, saliva, or embryo cells)
Laboratory processing and analysis
Report generation and counseling

How to Prepare for Genetic Testing

Preparation depends on the test. For blood or saliva tests, minimal preparation. For PGT, embryos are created via IVF and biopsied. For prenatal tests, timing and consent are discussed with your doctor.

Understanding Genetic Testing Results

Results are explained during genetic counseling. Normal results may rule out certain conditions; abnormal results help guide treatment, embryo selection, or pregnancy decisions. Our genetic counselors support you in understanding and next steps.

Cost of Genetic Testing

Cost varies by test type and number of samples or embryos. Contact us for a detailed quote and to book an appointment.