NIPT Microdeletion Test Cost AED:2400.0 – Symptoms, Diagnosis, and Details
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.
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.
| 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. |
