Prenatal test (NIFTY PLUS)
About
NIFTY PLUS is an advanced prenatal test that provides a comprehensive analysis of fetal DNA, offering a wider range of genetic information compared to the standard NIFTY test. It includes a more extensive assessment of chromosomal abnormalities, microdeletions, and other genetic conditions.
Candidate
The NIFTY PLUS test is recommended for pregnant women who desire a more comprehensive assessment of their fetus's genetic health. It may be particularly relevant for women over 35 or those with a family history of genetic disorders.
Preparation
Similar to the standard NIFTY test, no specific preparation is required before the test. However, it is important to follow any guidance provided by the healthcare provider.
Treatment
The NIFTY PLUS test involves collecting a sample of the mother's blood and analyzing the fetal DNA using next-generation sequencing (NGS) technology. This allows for a thorough assessment of the genetic health of the fetus, including the identification of various chromosomal abnormalities and microdeletions.
Result
The results of the NIFTY PLUS test provide detailed information on a wide range of genetic conditions, including chromosomal abnormalities, microdeletions, and other genetic disorders. These results can help guide the healthcare provider in providing appropriate counseling and developing a suitable plan for the management of the pregnancy.
Precautions
It is essential that the results of the NIFTY PLUS test are interpreted by a qualified genetic counselor or healthcare provider. Understanding the implications of the test results and potential follow-up actions is crucial to ensure appropriate care and management during the pregnancy.
F.A.Q.
NIPT is a non-invasive method that analyzes fetal DNA in the mother's blood to screen for certain genetic conditions and chromosomal abnormalities.
NIFTY PLUS is an advanced version of NIPT that provides screening for a wider range of genetic conditions, including common chromosomal disorders and some single-gene disorders.
NIFTY PLUS expands the scope of screening to include more genetic conditions beyond the standard chromosomal abnormalities.
NIFTY PLUS is typically conducted after the 10th week of pregnancy and can be done as part of routine prenatal screening.
NIFTY PLUS can detect a broader range of genetic conditions, including common chromosomal abnormalities, as well as some single-gene disorders.
NIFTY PLUS offers a more comprehensive screening, but the accuracy of the test still depends on the specific conditions being screened.
Yes, like other NIPT tests, NIFTY PLUS can determine the baby's gender with high accuracy.
NIFTY PLUS is considered safe, as it involves only a blood sample from the pregnant woman.
If your NIFTY PLUS results indicate an increased risk for a genetic condition, your healthcare provider may recommend further diagnostic testing to confirm the diagnosis and discuss potential options and next steps.
Yes, NIFTY PLUS has the capability to detect certain rare genetic disorders in addition to common chromosomal abnormalities. It screens for a broader range of genetic conditions, including some single-gene disorders that may not be covered by traditional prenatal tests. However, it's important to note that the scope of disorders detected can vary, so it's recommended to discuss with your healthcare provider to understand which conditions are included in the NIFTY PLUS screening panel.
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