Are you expecting a baby and want to ensure their health and well-being right from the start? Look no further than our ClariTest core state-of-the-art Non-Invasive Prenatal Testing (NIPT) services. With NIPT, you can gain valuable insights into your unborn child’s genetic makeup and identify potential health risks early on.
Join us on this incredible journey of discovery and make informed decisions for the future of your family!
Who should take the test:
Pregnant women, who would like to know, as accurately as possible, if their baby is healthy or not
ClariTest may also be an option that you can consider if the expectant mother is in one of of the following categories:
- High risk due to age (35 years at delivery).
- Ultrasound showing specific changes in growth and / or development of the baby.
- Abnormal or positive Triple Test results during the first or second quarter.
- Personal or family history of chromosomal disorders.
- Recommendation from obstetrician to perform this test, patients must be 18 years or older, with a singleton.
Why Consider the CalriTest Core NIPT service
Accurate and Reliable Testing
At Maitri, through our partnership with South Genetics, we pride ourselves on offering the most accurate and reliable NIPT services available. South Genetics advanced technology enables us to analyze fetal DNA in the maternal bloodstream with unmatched precision. You can trust us to provide you with the most accurate and comprehensive results, giving you peace of mind during this crucial time.
Early Detection of Genetic Conditions
NIPT allows for early detection of genetic conditions, such as Down syndrome, Edwards syndrome, and Patau syndrome, among others. By detecting these conditions early, you can better prepare for any potential challenges and make informed decisions about your baby’s healthcare needs.
Our expert genetic counselors will guide you through the process and help you understand the results, ensuring you have all the information you need to make the best choices for your family.
Non-Invasive and Safe
Unlike invasive procedures like amniocentesis, NIPT is non-invasive and poses no risk to the mother or the baby. It involves a simple blood draw from the mother, making it a safe and stress-free option for prenatal genetic testing. Our skilled and caring medical professionals will ensure a comfortable experience for you throughout the entire process.
Genetic Counseling Services
Learn more about our genetic counselling services
The Test
CalriTest Core prenatal test is a type of non-invasive prenatal test (NIPT). It looks at fragments of your baby’s DNA in your blood to provide accurate information about the likelihood for the most common chromosomal conditions from as early as 10 weeks. It also identifies the sex of your baby.
Chromosomal Conditions Tested
- Trisomies
- Trisomy 21 (Down syndrome)
- Trisomy 18 (Edwards syndrome)
- Trisomy 13 (Patau syndrome)
- Sex chromosome aneuploidies
- Monosomy X (Turner syndrome)
- XXY (Klinefelter syndrome)
- XXX (Triple X syndrome) – XYY and XXYY
Chromosomal Conditions
- Down syndrome (trisomy 21): This condition happens when a baby has an extra chromosome 21. It causes learning difficulties, slower development, and unique physical features like a flatter face and upward-slanting eyes.
- Edwards syndrome (trisomy 18): Babies with this condition have an extra chromosome 18. It leads to serious health problems and developmental delays, and many affected babies don’t live long.
- Patau syndrome (trisomy 13): This condition occurs when there’s an extra chromosome 13. It causes severe intellectual disability and physical problems, such as heart defects, and most babies with this condition have a very short lifespan.
- Turner Syndrome: This condition affects girls and happens when one of their X chromosomes is missing or incomplete. It can lead to shorter height, delayed puberty, and heart issues.
- Klinefelter syndrome: This condition affects boys who have an extra X chromosome. It can cause low testosterone levels, reduced muscle and body hair, and learning difficulties.
- Monosomy X (Turner Syndrome): This condition affects girls and occurs when one of their X chromosomes is missing. It can cause short height, delayed puberty, and heart problems. Girls with this condition might also have learning difficulties.
Take charge of your baby’s future by choosing our Maitri Diagnostics for your NIPT needs. Contact us today to schedule an appointment and embark on a journey of discovery. Trust our expertise and cutting-edge technology to provide you with the most accurate and reliable results. Give your baby the best start in life with NIPT at our Molecular Diagnostic Lab!
Test Details
- Sample Type: Blood
- Collection Method: In person at Maitri Diagnostics or at an authorized location
- Age: N/A
- Results: 15-20 days post sample
- Test must be taken by purchaser
Preparation: Does not require fasting or prior preparation. We strongly advise, however, that you stay hydrated.