Prenatal PREMIUM Test: T 21, 18, 13 + Sex Chromosomes + Microdeletions + Gender

The PREMIUM test, available at IntroLab in Belgrade, utilizes advanced technology to analyze fetal genetic material, offering a comprehensive assessment of potential genetic disorders and determining the baby’s gender. It is intended for parents who seek the most detailed information about their child’s genetic health to ensure the best possible prenatal care.

Why choose the PREMIUM test?

The PREMIUM test is designed to offer a more in-depth understanding of the fetus’s genetic health, covering a broad range of potential disorders. Parents who opt for this test gain valuable insights that help them better understand potential genetic risks and make informed decisions regarding future care and health planning.

What does the prenatal PREMIUM test include?

The PREMIUM Test covers the following aspects of genetic health:

• Trisomy detection: It screens for the most common trisomies, including Trisomy 21 (Down syndrome), Trisomy 18 (Edwards syndrome), and Trisomy 13 (Patau syndrome). These trisomies are linked to genetic disorders that can affect a child’s development and health.
• Sex chromosome analysis: It detects abnormalities in the sex chromosomes (X and Y), which can indicate disorders such as Turner syndrome or Klinefelter syndrome. This analysis helps identify conditions related to sex that may influence physical and cognitive development.
• Microdeletion detection: It screens for microdeletions—small missing segments of genetic material that can lead to serious health issues, including specific syndromes and developmental disorders. Although microdeletions may have subtle but significant health impacts, detecting them provides crucial information for planning prenatal and postnatal care.
• Gender determination: It accurately determines the baby’s gender, providing additional valuable information for parents.

Who is the PREMIUM test for?

The test is designed for:

• Couples with a history of geneticdisorders: Those with a family history of trisomies, sex chromosome abnormalities, or other genetic conditions.
• Pregnant women: Any expectant mother seeking a thorough analysis of her baby’s genetic health to ensure timely and appropriate medical care.
• Older pregnant women: Given the increased risk of genetic disorders with advancing maternal age, the PREMIUM test offers additional reassurance and valuable information.

How is the test performed?

The test involves taking a blood sample from the mother, from which fetal DNA fragments are isolated. This sample is then analyzed using advanced genome sequencing technology, enabling accurate detection of genetic abnormalities. The test is non-invasive, safe, and painless for both the mother and baby.

Prenatal genetic testing: Options at IntroLab

In addition to the PREMIUM test, IntroLab offers a range of prenatal tests tailored to meet the diverse needs of expecting parents:

• BASIC Test: Focuses on detecting the most common trisomies, such as Trisomy 21, 18, and 13, along with determining the baby’s gender.
• PLUS Test: This test includes trisomy detection along with the analysis of sex chromosomes, allowing for the identification of sex-specific genetic abnormalities.
• EXPERT Test: Includes everything in the PLUS Test, with the added analysis for DiGeorge syndrome, providing a more comprehensive view of the fetus’s genetic health.
• ALL CHROMOSOMES Test: Provides a detailed analysis of all chromosomes, including sex chromosomes, deletions, microdeletions, and gender determination.
• SPECIAL Test: An expanded analysis that covers trisomies, sex chromosomes, microdeletions, and screening for 100 hereditary diseases.

These tests use advanced genetic technology to provide accurate and reliable information.

Advanced genetic panels at IntroLab

In addition to prenatal tests, we offer a range of specialized genetic panels that use NGS technology:

• Autoinflammatory diseases panel
• Cardiomyopathy panel
• Arrhythmia panel
• Marfan syndrome panel
• Epilepsy panel
• Clinical exome sequencing
• Molecular karyotyping

With these panels, you can obtain precise genetic insights, allowing doctors to provide the best possible care.