Longevity.haus

Non-Invasive Fetal Sex Determination

Type

Genetic Testing

Duration

15 min

Sample

Blood (maternal venous)

What's included

3 deliverables in this treatment

  • Maternal venous blood draw
  • Analysis for Y-chromosome (SRY) DNA in maternal blood
  • Written laboratory result report

This non-invasive test determines the sex of the fetus by detecting Y-chromosome (SRY gene) DNA fragments in a maternal blood sample. It requires only a routine blood draw and can be performed from early in pregnancy, giving expectant parents an early and reliable answer without any invasive procedure. The same SRY detection method is also offered as a standalone test, for example for sport eligibility verification.

About this treatment

Early fetal sex determination uses the same cell-free fetal DNA principle as non-invasive prenatal screening. A maternal blood sample is analysed for the presence of Y-chromosome-specific sequences, most notably the SRY gene. Detection of Y-chromosome DNA indicates a male fetus; its absence indicates a female fetus. Because fetal DNA is present in maternal blood from early in pregnancy, the test can give a result well before sex is visible on ultrasound.

The laboratory performs the analysis from a standard venous blood draw with no risk to the pregnancy. The same SRY-detection assay is also available as a standalone genetic test outside of pregnancy contexts. The test is intended for expectant parents who want to know fetal sex early, and for situations where a clinical reason makes early sex determination useful, such as families with a history of sex-linked genetic conditions.

Good to know

Sample
Maternal blood draw (non-invasive)
Method
SRY / Y-chromosome DNA detection
Timing
Available early in pregnancy

Who is this for?

Expectant parents wanting early fetal sex; families with a history of sex-linked genetic conditions

About the clinic

Reviews, team and credentials

Independent review links and clinic-reported team information.

Clinical team

The laboratory is headed by RNDr. Jitka Kadlecová, Ph.D., supported by a team of cytogenetic and molecular genetic specialists with long-term laboratory experience in prenatal and postnatal genetic diagnostics.

Languages: Czech, English

View the full Cytogenetická laboratoř Brno profile
Compare Genetic Testing in Czechia →