NIPT Test in KL & Selangor
NIPT Prenatal Screening at Dr Prevents Clinic
At Dr. Prevents, we know that pregnancy can be both exciting and worrying for parents-to-be. That’s why we focus on providing advanced prenatal care to keep both mom and baby healthy. Our Non-Invasive Prenatal Testing (NIPT) offers valuable insights into the baby’s genetic health with a simple blood test.
What is the NIPT Test?
NIPT, short for Non-Invasive Prenatal Testing, is an advanced screening method that analyzes fetal DNA found in the mother’s blood. This test can identify the likelihood of specific chromosomal abnormalities, including Down syndrome (Trisomy 21), Edwards syndrome (Trisomy 18), Patau syndrome (Trisomy 13), and irregularities in the number of sex chromosomes (like Turner syndrome or Klinefelter syndrome).
The NIPT test checks for chromosomal abnormalities by examining the amount of fetal DNA in the mother’s blood. This DNA comes from the placenta during pregnancy. NIPT is safe and non-invasive, meaning it doesn’t pose any risk to the mother or baby. All that’s needed for the test is a simple blood sample from the mother.
Why Choose Non-Invasive Prenatal Tests?
Accuracy
NIPT boasts high levels of accuracy in detecting common chromosomal abnormalities, with a low rate of false positives.
Safety
Unlike traditional invasive prenatal tests, such as amniocentesis or chorionic villus sampling (CVS), NIPT does not pose any risk of miscarriage or harm to the fetus.
Early Detection
NIPT can be performed as early as 9-10 weeks into the pregnancy, providing expectant parents with timely information about their baby's health.
Who Should Consider NIPT?
NIPT tests are recommended for pregnant women who fall into one or more of the following categories:
Pregnant individuals aged 35 or older: Older pregnant women have a higher risk of chromosomal abnormalities like Down syndrome (Trisomy 21), making them potential candidates for NIPT.
Women with positive screening results: Those who received positive results from other prenatal screening tests, such as first-trimester combined screening or maternal serum screening, may opt for NIPT to gather additional information and clarify risk.
Individuals with a history of chromosomal abnormalities: Those who have experienced a previous pregnancy affected by chromosomal abnormalities may choose NIPT for early detection and planning in subsequent pregnancies.
Those with known genetic conditions or family history: Pregnant individuals with known genetic conditions or a family history of chromosomal abnormalities may consider NIPT for extra reassurance and planning.
It’s crucial to understand that while NIPT is highly accurate as a screening test, it isn’t a diagnostic tool. Positive results should be confirmed with further diagnostic testing, such as amniocentesis or chorionic villus sampling (CVS), to provide a definitive diagnosis. Additionally, NIPT may not be suitable for all pregnancies, so it’s essential to discuss the options with your doctor here at our clinic to determine the most appropriate screening strategy based on individual circumstances and preferences.
What to Expect During NIPT
Pre-Test Counseling
Before undergoing NIPT, expectant parents will typically receive genetic counseling to discuss the test's purpose, benefits, and limitations.
Blood Draw
A small blood sample will be collected from the mother's arm using a standard venipuncture procedure. This process is quick and relatively painless.
Laboratory Analysis
The blood sample will be sent to our lab, where our trained technicians will extract and analyze the fetal DNA.
Results
Typically, results are available within 7 working days. A healthcare provider will discuss the findings with the parents and provide appropriate guidance and support
Commonly Detected Diseases
Down Syndrome: A genetic disorder caused by the presence of an extra copy of chromosome 21, resulting in developmental delays, intellectual disability, and distinct physical features such as slanted eyes and a flattened face.
Edwards Syndrome: Also known as Trisomy 18, it is a chromosomal disorder caused by an extra copy of chromosome 18. Individuals with Edwards syndrome often have severe developmental delays, heart defects, and characteristic physical abnormalities such as clenched fists and overlapping fingers.
Patau Syndrome: Also known as Trisomy 13, it is a chromosomal disorder caused by an extra copy of chromosome 13. Patau syndrome is characterized by severe intellectual disability, heart defects, and physical abnormalities such as cleft lip and palate, extra fingers or toes, and brain abnormalities.
Klinefelter Syndrome: A genetic condition in males caused by the presence of an extra X chromosome, resulting in infertility, underdeveloped testes, and may lead to reduced muscle mass, tall stature, and learning disabilities.
Triple X Syndrome: A genetic condition in females characterized by the presence of an extra X chromosome, resulting in variable symptoms such as tall stature, learning disabilities, delayed development, and may increase the risk of certain health conditions such as autoimmune disorders and behavioral issues.
Why Choose Dr. Prevents to Get Your NIPT Test?
24-hour Response
Receive the best immediate care. Whether it's the middle of the night or a weekend, a 24-hour clinic is there for you when unexpected health issues arise.
Accessibility
With multiple clinic locations in KL and Selangor, we ensure ease of accessibility with a provided wheelchair ramp. Please let us know prior to your arrival, and our dedicated staff will be ready to assist you.
Expert Care and Support
When you choose Dr. Prevent's Clinic for your NIPT test, you our team of healthcare professionals is committed to delivering accurate results, timely diagnosis, and personalized care to help you achieve your health goals.
