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Chromotouch Chromosome SNP Microarray Optima Prenatal Test Cost

Original price was: 3,900 د.إ.Current price is: 3,510 د.إ.

-10%

The “Chromotouch Chromosome SNP Microarray Optima Prenatal Test” is an advanced prenatal screening test available at DNA Labs UAE, designed to detect chromosomal abnormalities in a fetus with high accuracy. This non-invasive test examines single nucleotide polymorphisms (SNPs) across the genome, providing detailed information about the chromosomal health of the fetus. It can identify various genetic conditions, including Down syndrome, Edwards syndrome, Patau syndrome, and other chromosomal anomalies that could affect the baby’s development.

Performed using a simple blood draw from the expectant mother, this test poses no risk to the fetus, making it a preferred choice for many parents-to-be who seek peace of mind regarding their unborn child’s genetic health. The Chromotouch technology ensures a comprehensive analysis by examining millions of data points across the fetal genome, offering a clearer picture than traditional prenatal screening methods.

The test is priced at 3510 AED, reflecting the advanced technology and detailed insights it provides. Conducted at the state-of-the-art facilities of DNA Labs UAE, clients are assured of accurate results, professional service, and confidentiality. This test is a valuable tool for expecting parents who wish to have early and precise information about their baby’s chromosomal health, allowing them to make informed decisions regarding their pregnancy.

Home  Sample collection service available

  • 100% accuaret Test Results
  • Ranked as Most trusted Genetic DNA Lab
  • This test is not intended for medical diagnosis or treatment
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CHROMOTOUCH CHROMOSOME SNP MICROARRAY OPTIMA PRENATAL Test

Cost: AED 3510.0

Test Components

  • Price: AED 3510.0
  • Sample Condition:
    • Amniotic fluid: 15 mL (10 mL min.) in a sterile screw capped container.
    • Chorionic villus: 30 mg (20 mg min.) biopsy collected aseptically in 10 mL transport medium available from LPL.
    • Umbilical Cord blood: 4 mL (2 mL min.) cord blood in 1 Lavender top (EDTA) tube. Avoid clot formation during sampling. Ship refrigerated immediately. DO NOT FREEZE.
  • Duly filled Genomic Microarray Requisition Form (Form 19) & Consent form (Form 18) for Prenatal genetic testing is mandatory.

Report Delivery

Sample Daily by 4 pm; Report 10 Working days

Method

Affymetrix Optima Suite Microarray

Test Type

Genetic Disorders

Doctor

Gynecologist

Test Department

CYTOGENETICS

Pre Test Information

Duly filled Genomic Microarray Requisition Form (Form 19) & Consent form (Form 18) for Prenatal genetic testing is mandatory.

Test Details

The CHROMOTOUCH CHROMOSOME SNP MICROARRAY OPTIMA PRENATAL Test is a prenatal genetic test that analyzes the chromosomes of a fetus to detect any abnormalities or genetic disorders. It uses a microarray technology that examines single nucleotide polymorphisms (SNPs) across the genome to identify any variations or deletions in the chromosomes.

This test is performed on a sample of amniotic fluid or chorionic villus sampling (CVS) tissue, which is collected during pregnancy. It can provide information about the baby’s risk for genetic conditions such as Down syndrome, Edwards syndrome, Patau syndrome, and other chromosomal abnormalities.

The CHROMOTOUCH CHROMOSOME SNP MICROARRAY OPTIMA PRENATAL Test offers high accuracy and sensitivity in detecting genetic abnormalities, providing expectant parents with valuable information about their baby’s health and potential medical conditions. This information can help guide decisions about prenatal care and treatment options.

It is important to note that this test is typically recommended for women with a higher risk of having a baby with a chromosomal abnormality, such as advanced maternal age or a family history of genetic disorders. It is always advised to consult with a healthcare professional or genetic counselor to determine if this test is appropriate for an individual’s specific situation.

Test Name CHROMOTOUCH CHROMOSOME SNP MICROARRAY OPTIMA PRENATAL Test
Components
Price 3510.0 AED
Sample Condition Amnotic fluid: 15 mL (10 mL min.) in a sterile screw capped container.\n Chorionic villus: 30 mg (20 mg min.) biopsy collected asceptically in 10 mL transport medium available from LPL.Umblical Cord blood: 4 mL (2 mL min.) cord blood in 1 Lavender top (EDTA) tube. Avoid clot formation during sampling. Ship refrigerated immediately.DO NOT FREEZE. Duly filled Genomic Microarray Requisition Form (Form 19) & Consent form (Form 18) for Prenatal genetic testing is mandatory.
Report Delivery Sample Daily by 4 pm; Report 10 Working days
Method Affymetrix Optima Suite? Microarray
Test type Genetic Disorders
Doctor Gynecologist
Test Department: CYTOGENETICS
Pre Test Information Duly filled Genomic Microarray Requisition Form (Form 19) & Consent form (Form 18) for Prenatal genetic testing is mandatory.
Test Details

The CHROMOTOUCH CHROMOSOME SNP MICROARRAY OPTIMA PRENATAL Test is a prenatal genetic test that analyzes the chromosomes of a fetus to detect any abnormalities or genetic disorders. It uses a microarray technology that examines single nucleotide polymorphisms (SNPs) across the genome to identify any variations or deletions in the chromosomes.

This test is performed on a sample of amniotic fluid or chorionic villus sampling (CVS) tissue, which is collected during pregnancy. It can provide information about the baby’s risk for genetic conditions such as Down syndrome, Edwards syndrome, Patau syndrome, and other chromosomal abnormalities.

The CHROMOTOUCH CHROMOSOME SNP MICROARRAY OPTIMA PRENATAL Test offers high accuracy and sensitivity in detecting genetic abnormalities, providing expectant parents with valuable information about their baby’s health and potential medical conditions. This information can help guide decisions about prenatal care and treatment options.

It is important to note that this test is typically recommended for women with a higher risk of having a baby with a chromosomal abnormality, such as advanced maternal age or a family history of genetic disorders. It is always advised to consult with a healthcare professional or genetic counselor to determine if this test is appropriate for an individual’s specific situation.

SKU: TEST-4720 Category:

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