Chromotouch Chromosome SNP Microarray Optima Prenatal Test
Introduction
The Chromotouch Chromosome SNP Microarray Optima Prenatal Test is an advanced genetic screening tool that plays a critical role in prenatal care. This test is designed to detect chromosomal abnormalities in a developing fetus, providing essential information that can aid in the management of pregnancy and the health of the newborn. With the increasing awareness of genetic disorders, this test is becoming an invaluable resource for expectant parents.
What the Test Measures
This test utilizes state-of-the-art microarray technology to analyze the chromosomes of the fetus. It detects single nucleotide polymorphisms (SNPs) that may indicate potential genetic disorders. By examining these chromosomal markers, healthcare providers can identify conditions such as Down syndrome, Turner syndrome, and other genetic anomalies.
Who Should Consider This Test
Expectant parents who are at risk of genetic disorders or have a family history of such conditions should consider the Chromotouch Chromosome SNP Microarray Optima Prenatal Test. Additionally, individuals over the age of 35, those with previous pregnancies affected by genetic disorders, or couples with a known history of chromosomal abnormalities may benefit from this test.
Benefits of Taking the Test
- Early detection of potential genetic disorders.
- Informed decision-making regarding pregnancy management.
- Peace of mind for expectant parents.
- Access to appropriate medical care and interventions if needed.
Understanding Your Results
After the test is conducted, results will be available within 10 working days. Your healthcare provider will guide you through the interpretation of the results. It is important to understand that while the test can identify certain genetic disorders, it does not provide definitive answers for all conditions. Further testing may be recommended based on the findings.
Test Name and Price
| Discount Price | 370,000 NGN |
|---|---|
| Regular Price | 500,000 NGN |
Booking the Test
To book the Chromotouch Chromosome SNP Microarray Optima Prenatal Test, please ensure you have a duly filled Genomic Microarray Requisition Form (Form 19) and Consent Form (Form 18) for prenatal genetic testing. Sample collection can be done using:
- 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.
For further inquiries or to schedule your appointment, please call or WhatsApp us at +2348077798758.