Comprehensive Guide to Noninvasive Prenatal Testing for Fetal Chromosomal Aneuploidies and Microduplications / Microdeletions (NIPT-Plus)

NIPT-Plus is an advanced screening method that analyzes fetal DNA circulating in a pregnant woman’s blood. This test is designed to detect not only common chromosomal abnormalities, such as fetal chromosomal aneuploidies, but also smaller genetic deletions / duplications known as microdeletions / microduplications. CapitalBiotech’s NIPT-Plus is a state-of-the-art solution that offers comprehensive screening for both aneuploidies and microdeletions / microduplications, providing healthcare providers with reliable and accurate results.

What are Microdeletions / Microduplications in Pregnancy?

Microdeletions / microduplications in pregnancy refer to missing/duplication of small segments of DNA within a chromosome that can lead to genetic disorders. These deletions/duplications are often too small to be detected by traditional karyotyping methods. However, they can have significant impacts on a child’s development and health. Conditions such as DiGeorge syndrome (22q11.2 deletion) and Williams syndrome (7q11.23 deletion) are examples of disorders caused by microdeletions / microduplications. CapitalBiotech’s NIPT-Plus test is specifically designed to identify these small but critical genetic changes, offering a more detailed and accurate prenatal screening option.

What are Aneuploidies?

Aneuploidies are genetic conditions where there is an abnormal number of chromosomes in a cell. Instead of the typical 46 chromosomes, an individual with aneuploidy may have one extra or one missing chromosome. This imbalance can lead to various developmental and health issues. Common examples of aneuploidies include Down syndrome (trisomy 21), Edwards syndrome (trisomy 18), and Patau syndrome (trisomy 13). CapitalBiotech’s fetal chromosomal NIPT-Plus test is designed to detect these abnormalities with high accuracy, providing essential information for prenatal care.

What are the 4 Types of Aneuploidies?

1. Monosomy: This occurs when there is a missing chromosome in a pair. For example, Turner syndrome is a condition where a female has only one X chromosome instead of two.

2. Trisomy: This is a genetic condition characterized by the presence of an extra chromosome. Down syndrome (trisomy 21) is the most well-known example, where there is an extra copy of chromosome 21.

3. Tetrasomy: This rare condition involves the presence of two extra chromosomes. An example is tetrasomy 18p, where there are four copies of the short arm of chromosome 18.

4. Nullisomy: This extremely rare condition involves the absence of both chromosomes in a pair. Nullisomy is usually lethal and not compatible with life.

CapitalBiotech’s NIPT-plus is capable of detecting these various types of aneuploidies, providing comprehensive screening for expectant parents.

What is the Most Common Fetal Aneuploidy?

The most common fetal aneuploidy is Down syndrome, also known as trisomy 21. This condition occurs when there is an extra copy of chromosome 21, leading to developmental delays, intellectual disabilities, and various health issues. Down syndrome is the most frequently occurring chromosomal abnormality detected in prenatal screenings. CapitalBiotech’s NIPT-Plus test is highly effective in identifying Down syndrome, along with other common aneuploidies, providing crucial information for expectant parents and healthcare providers.

Conclusion

CapitalBiotech’s NIPT-Plus offers a comprehensive solution for prenatal screening, detecting both fetal chromosomal aneuploidy and microdeletions / microduplications with high accuracy. By understanding the complexities of genetic disorders such as aneuploidies and microdeletions / microduplications, healthcare providers can offer better care and support to expectant parents. CapitalBiotech’s advanced testing methods ensure that critical genetic information is obtained early in pregnancy, allowing for informed decision-making and improved outcomes. Choose CapitalBiotech for cutting-edge and reliable prenatal screening.

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