Chromosomal disorders: such as Down syndrome (chromosome 21), Edwards syndrome (chromosome 18), and Patau syndrome (chromosome 13). Genetic composition of the fetus: helps identify genetic changes that may indicate health or hereditary issues. Fetal sex determination: the test can reveal the baby’s sex based on the DNA present in the mother’s blood. Risk assessment for disorders: provides results indicating the likelihood of certain disorders, helping parents make informed decisions about the pregnancy and healthcare.

Pregnant women in early stages of pregnancy, typically after the 10th week of gestation. Women with a family history of genetic disorders, making them more susceptible to certain conditions. Women who have shown abnormal results in previous screenings, such as the triple blood test or ultrasound. Women over the age of 35, as the risk of chromosomal abnormalities increases with maternal age. Women who want accurate information about their baby’s health and prefer a non-invasive test to avoid risks associated with invasive procedures.

Maternal age: Women over 35 years old are at higher risk for chromosomal abnormalities. Abnormal results in previous screenings: If tests such as the triple blood test or ultrasound indicate a potential issue. Family history of genetic disorders: A family history of inherited conditions may warrant the test. Maternal concern about fetal health: The desire for reassurance about the baby's health before birth.

How does the NIPT test work? The test analyzes fetal DNA present in the mother's blood sample, allowing detection of chromosomal abnormalities. When can the test be performed? It is recommended to perform NIPT after the 10th week of pregnancy for accurate results. Is this test safe? Yes, NIPT is a non-invasive test, meaning it does not require invasive procedures such as amniocentesis. How accurate are the results? NIPT is very accurate, but it is not a substitute for diagnostic tests like amniocentesis or chorionic villus sampling. What do positive and negative results mean? A positive result indicates a potential risk for a chromosomal disorder, while a negative result means the risk is low. Can the test produce errors? Despite its high accuracy, errors can occur. Confirmatory testing is recommended if abnormal results are found. Does insurance cover this test? Coverage varies depending on insurance plans. It is advised to check with your healthcare provider. What should be done after receiving the results? Discuss the results with a specialist to understand the available options and conduct further testing if necessary.

Negative result: Indicates a low likelihood of chromosomal abnormalities such as Down syndrome, meaning the results are considered normal. Positive result: Indicates a potential risk for a chromosomal disorder, such as Down syndrome, but does not necessarily mean the fetus is affected. Probabilistic results: Provide a percentage or ratio indicating the likelihood of the disorder (e.g., 1 in 1000, or 1 in 100).

NIPT Genetic Test Price | Lahalak Medical Platform

A safe maternal blood test analyzing fetal DNA for early detection of genetic syndromes like Down syndrome, giving you complete peace of mind about your baby's health.

Prices starts from: 1008 SAR

Scientific name: Non-Invasive Prenatal Testing (NIPT)

NIPT Test (Non-Invasive Prenatal Testing) is an advanced test used to examine the genetic status of the fetus by analyzing fetal DNA found in a sample of the mother’s blood. This test is a safe and non-invasive method to detect potential genetic disorders, such as Down syndrome and other chromosomal abnormalities. NIPT is usually performed after th...

Non-Invasive Prenatal Testing (NIPT) - Early Fetal Genetic Screening

Service type Genetic test (Blood)

Duration 10-15 minutes

Fasting Fasting is not required

Prices Starting from 1008 SAR

Included Services

NIPT Test (Non-Invasive Prenatal Testing for Fetal DNA Detection) Test
The optimal health guidance based on the result.
Personal support services from Lahalak

Medical Service Information

Purpose Test

Chromosomal disorders: such as Down syndrome (chromosome 21), Edwards syndrome (chromosome 18), and Patau syndrome (chromosome 13).
Genetic composition of the fetus: helps identify genetic changes that may indicate health or hereditary issues.
Fetal sex determination: the test can reveal the baby’s sex based on the DNA present in the mother’s blood.
Risk assessment for disorders: provides results indicating the likelihood of certain disorders, helping parents make informed decisions about the pregnancy and healthcare.

Recommended groups

Pregnant women in early stages of pregnancy, typically after the 10th week of gestation.
Women with a family history of genetic disorders, making them more susceptible to certain conditions.
Women who have shown abnormal results in previous screenings, such as the triple blood test or ultrasound.
Women over the age of 35, as the risk of chromosomal abnormalities increases with maternal age.
Women who want accurate information about their baby’s health and prefer a non-invasive test to avoid risks associated with invasive procedures.

Symptoms indicative

Maternal age: Women over 35 years old are at higher risk for chromosomal abnormalities.
Abnormal results in previous screenings: If tests such as the triple blood test or ultrasound indicate a potential issue.
Family history of genetic disorders: A family history of inherited conditions may warrant the test.
Maternal concern about fetal health: The desire for reassurance about the baby's health before birth.

FAQs

How does the NIPT test work? The test analyzes fetal DNA present in the mother's blood sample, allowing detection of chromosomal abnormalities.
When can the test be performed? It is recommended to perform NIPT after the 10th week of pregnancy for accurate results.
Is this test safe? Yes, NIPT is a non-invasive test, meaning it does not require invasive procedures such as amniocentesis.
How accurate are the results? NIPT is very accurate, but it is not a substitute for diagnostic tests like amniocentesis or chorionic villus sampling.
What do positive and negative results mean? A positive result indicates a potential risk for a chromosomal disorder, while a negative result means the risk is low.
Can the test produce errors? Despite its high accuracy, errors can occur. Confirmatory testing is recommended if abnormal results are found.

Normal Levels

Negative result: Indicates a low likelihood of chromosomal abnormalities such as Down syndrome, meaning the results are considered normal.
Positive result: Indicates a potential risk for a chromosomal disorder, such as Down syndrome, but does not necessarily mean the fetus is affected.
Probabilistic results: Provide a percentage or ratio indicating the likelihood of the disorder (e.g., 1 in 1000, or 1 in 100).