Prenatal ALL CHROMOSOMES Test: ALL CHROMOSOMES + Sex Chromosomes + Deletions and Microdeletions + Gender

The ALL CHROMOSOMES test is an advanced prenatal test offering a detailed assessment of your unborn child’s genetic health. It is designed to analyze all chromosomes, including sex chromosomes, and detect significant deletions and microdeletions. Additionally, it determines the fetus’s gender, providing an extra advantage for parents who wish to plan ahead.

What does the ALL CHROMOSOMES test include?

The ALL CHROMOSOMES test offers a comprehensive analysis of chromosomes, covering:

• Detection of aneuploidies: This includes chromosomal disorders like Trisomy 21 (Down syndrome), Trisomy 18 (Edwards syndrome), and Trisomy 13 (Patau syndrome).
• Sex chromosome analysis: It identifies abnormalities such as Turner syndrome (Monosomy X), Klinefelter syndrome (XXY), and other variations involving the X and Y chromosomes.
• Microdeletions and deletions: The test also detects specific microdeletions, such as the 22q11.2 deletion associated with DiGeorge syndrome, along with other chromosomal deletions that can cause significant health problems.

Why choose the ALL CHROMOSOMES test?

Opting for this test provides several benefits:

• Comprehensive analysis: This test offers a thorough assessment of chromosomal abnormalities, including less common issues like microdeletions.
• High accuracy: With the use of advanced Next-Generation Sequencing (NGS) technology, the test provides highly accurate results, minimizing the chance of errors.
• Non-invasive: The test is completely safe, requiring only a blood sample from the mother, with no risk to the baby
• Early detection: The test can be conducted as early as the 10th week of pregnancy, enabling the early identification of potential issues and timely planning for further action.

Results and expectations

The results of the ALL CHROMOSOMES test are typically available within 10 business days. They offer a detailed assessment of the risk for various chromosomal abnormalities. If the test indicates an elevated risk for any abnormality, further diagnostic tests, such as amniocentesis, are recommended to confirm the findings.

Who is the ALL CHROMOSOMES test for?

This test is ideal for:

• Pregnant women over 35, who are at an increased risk for chromosomal abnormalities.
• Individuals with a family history of genetic disorders.
• Pregnant women who have had previous pregnancies with chromosomal abnormalities.
• Anyone seeking the most comprehensive analysis available for reassurance during pregnancy.

Price of the ALL CHROMOSOMES test

The ALL CHROMOSOMES test costs 100,182 RSD. This price includes a comprehensive analysis of all chromosomes, sex chromosomes, and the detection of microdeletions and other significant genetic disorders.

Additional prenatal tests and genetic analyses

In addition to the ALL CHROMOSOMES test, IntroLab offers a variety of other prenatal tests that provide early and accurate analysis of the fetus’s genetic health:

• Prenatal BASIC Test
• Prenatal PLUS Test
• Prenatal EXPERT Test
• Prenatal PREMIUM Test
• Prenatal SPECIAL Test
• Prenatal SPECIAL + SMA Test

In addition to prenatal tests, specialized genetic panels are also available:

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

All of these prenatal tests and genetic panels utilize advanced NGS technology to ensure precise results.