Chromosome Analysis High Resolution Neonatal Test
Introduction
The Chromosome Analysis High Resolution Neonatal Test is a vital diagnostic tool that helps in identifying genetic disorders in newborns. Conducted by a specialized team in Cytogenetics, this test utilizes advanced techniques such as culture, microscopy, and high-resolution karyotyping to examine the chromosomal structure of infants. Early detection of chromosomal abnormalities can lead to timely interventions, significantly improving health outcomes.
What the Test Measures
This test measures the number and structure of chromosomes in a newborn’s blood sample. It can detect various genetic disorders, including Down syndrome, Turner syndrome, and other chromosomal abnormalities that may affect the child’s development and health.
Who Should Consider This Test?
Parents may consider the Chromosome Analysis High Resolution Neonatal Test if:
- The baby shows symptoms of genetic disorders.
- There is a family history of genetic conditions.
- The pregnancy was complicated or there were abnormalities detected during ultrasound examinations.
- The mother is over 35 years old, increasing the risk of chromosomal abnormalities.
Benefits of Taking the Test
- Early identification of genetic disorders can lead to prompt medical management.
- Provides peace of mind for parents regarding their child’s health.
- Helps in planning for any special care or interventions needed for the child.
- Contributes to better understanding and research of genetic conditions.
Understanding Your Results
Results from the Chromosome Analysis High Resolution Neonatal Test will typically be available within 21 working days. A healthcare professional will guide you through the results, explaining any abnormalities detected and discussing potential implications for your child’s health.
Test Details and Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| Chromosome Analysis High Resolution Neonatal Test | 86580 NGN | 96200 NGN |
Pre-Test Instructions
It is recommended to conduct this test between 18-20 weeks of gestation. A duly filled Chromosome & FISH Analysis Requisition form (Form 17) is mandatory. The sample type required is 4 ml (2 ml min) of whole blood in a green top (Sodium Heparin) tube, which should be shipped refrigerated immediately. Please do not freeze the sample.
Book Your Test Today!
Don’t wait for signs of genetic disorders to appear. Ensure your newborn’s health and well-being by booking the Chromosome Analysis High Resolution Neonatal Test today. For appointments, please call or WhatsApp us at +2348077798758.
