NIPT Microdeletion Test Price 2400 AED – Symptoms, Diagnosis and Details
Decoding the Intricacies: Grasping the NIPT Microdeletion Test in the UAE
Pregnancy is a journey filled with joy, yet it also brings a natural inclination to ensure the wellbeing of your unborn child. The Non-Invasive Prenatal Test (NIPT) Microdeletion Test serves as a significant resource for prospective parents in the UAE. This progressive test transcends conventional NIPT, offering a more comprehensive examination for chromosomal irregularities that could lead to developmental setbacks or congenital anomalies. Let’s delve deeper into the NIPT Microdeletion Test, its elements, and its role in prenatal healthcare.
What Exactly are Microdeletions?
Microdeletions refer to minuscule absent segments of chromosomes, which can occasionally result in health issues in a developing fetus. Conventional NIPT tests primarily concentrate on trisomies, where there is an additional chromosome. The NIPT Microdeletion Test specifically scrutinizes these absent chromosomal sections.
Indications of Microdeletion Syndromes:
It’s crucial to comprehend that:
- Not all microdeletions result in observable symptoms.
- Symptoms can significantly vary based on the specific chromosomal region impacted.
Some potential indications may encompass:
- Intellectual impairment
- Developmental lags
- Congenital anomalies
- Facial irregularities
Elements of the NIPT Microdeletion Test:
This progressive NIPT examines fetal cell-free DNA present in the mother’s bloodstream. It utilizes advanced technology to identify absent chromosomal sections associated with recognized microdeletion syndromes.
Pre-Test Insights:
- Who can benefit: This test might be suggested for expectant mothers with:
- A family history of microdeletion syndromes
- Elevated risk of chromosomal irregularities based on conventional NIPT results
- Worries about potential developmental lags in the fetus
- Advantages: Early detection facilitates further assessment and informed decision-making regarding pregnancy management.
Test Specifications:
- Sample: A straightforward blood draw from the mother is typically employed.
- Procedure: The blood sample undergoes sophisticated analysis to identify absent chromosomal sections.
- Turnaround Time: Results are generally accessible within one to two weeks.
Significance of the NIPT Microdeletion Test:
- Early Insights: This test provides a more profound level of information compared to conventional NIPT, potentially unveiling microdeletion concerns earlier in pregnancy.
- Informed Decisions: Early detection enables parents to make informed decisions about prenatal care, potential additional testing, and future planning.
- Peace of Mind: A negative test result can offer substantial reassurance for expecting parents.
Accessing the NIPT Microdeletion Test in the UAE:
The NIPT Microdeletion Test is progressively becoming accessible at esteemed diagnostic laboratories in the UAE. It’s vital to consult with your doctor to ascertain if this advanced test is suitable for you. They can provide a recommendation to a reliable facility offering the test.
Empowering Your Pregnancy Journey:
The NIPT Microdeletion Test empowers expecting parents in the UAE to gain valuable insights into their baby’s health. By discussing this test with your doctor and considering it if appropriate, you can contribute to a more informed and potentially less stressful pregnancy journey.
Test Details
NIPT (Non-Invasive Prenatal Testing) Microdeletion is a type of prenatal genetic testing that screens for certain genetic conditions in a developing fetus. Microdeletions are small deletions of genetic material that can cause various genetic disorders, such as DiGeorge syndrome, Angelman syndrome, and Prader-Willi syndrome.
NIPT Microdeletion uses a sample of the mother’s blood to analyze fetal DNA and detect any abnormalities. It is a non-invasive test, which means that it does not require any invasive procedures, such as amniocentesis or chorionic villus sampling (CVS).
NIPT Microdeletion is typically offered to women who are at an increased risk of having a baby with a genetic disorder, such as those who are over 35 years old, have a family history of genetic disorders, or have had a previous pregnancy with a genetic disorder.
Test Name: NIPT Microdeletion Test
Components: Streck Tube
Price: 2400 AED
Sample Condition: Peripheral blood (10 ml.)
Report Delivery: 8-10 working days
Method: NGS
Test Type: Genetics
Doctor: General Physician
Test Department: Pre Test Information
NIPT Microdeletion can be done with a Doctor’s prescription. Prescription is not applicable for surgery and pregnancy cases or people planning to travel abroad.
The results of NIPT Microdeletion can provide parents with important information about their baby’s health and help them make informed decisions about their pregnancy. However, it is important to note that NIPT Microdeletion is a screening test and not a diagnostic test. If an abnormality is detected, further testing, such as amniocentesis or CVS, may be recommended to confirm the diagnosis.
| Test Name | NIPT Microdeletion Test |
|---|---|
| Components | Streck Tube |
| Price | 2400 AED |
| Sample Condition | Peripheral blood (10 ml.) |
| Report Delivery | 8-10 working days |
| Method | NGS |
| Test type | Genetics |
| Doctor | General Physician |
| Test Department: | |
| Pre Test Information | NIPT Microdeletion can be done with a Doctors prescription. Prescription is not applicable for surgery and pregnancy cases or people planing to travel abroad. |
| Test Details | NIPT (Non-Invasive Prenatal Testing) Microdeletion is a type of prenatal genetic testing that screens for certain genetic conditions in a developing fetus. Microdeletions are small deletions of genetic material that can cause various genetic disorders, such as DiGeorge syndrome, Angelman syndrome, and Prader-Willi syndrome. NIPT Microdeletion uses a sample of the mother’s blood to analyze fetal DNA and detect any abnormalities. It is a non-invasive test, which means that it does not require any invasive procedures, such as amniocentesis or chorionic villus sampling (CVS). NIPT Microdeletion is typically offered to women who are at an increased risk of having a baby with a genetic disorder, such as those who are over 35 years old, have a family history of genetic disorders, or have had a previous pregnancy with a genetic disorder. The results of NIPT Microdeletion can provide parents with important information about their baby’s health and help them make informed decisions about their pregnancy. However, it is important to note that NIPT Microdeletion is a screening test and not a diagnostic test. If an abnormality is detected, further testing, such as amniocentesis or CVS, may be recommended to confirm the diagnosis. |
