Chromosome Analysis High Resolution Neonatal Test
Introduction
The Chromosome Analysis High Resolution Neonatal Test is a vital diagnostic tool designed to detect genetic disorders in newborns. This highly specialized test utilizes advanced techniques to analyze chromosomes, providing critical information that can influence medical decisions and interventions. Conducted by experienced professionals in the field of cytogenetics, this test is essential for parents seeking to understand their child’s genetic health early on.
What the Test Measures
This test measures the number and structure of chromosomes in a sample of blood. It detects any chromosomal abnormalities that may lead to genetic disorders, allowing for early diagnosis and management. The high-resolution aspect of the test ensures that even the smallest chromosomal changes are identified.
Who Should Consider This Test?
Parents should consider the Chromosome Analysis High Resolution Neonatal Test if:
- There is a family history of genetic disorders.
- The pregnancy is classified as high-risk due to maternal age or other factors.
- Ultrasound findings suggest potential chromosomal abnormalities.
- There are concerns regarding developmental delays or other health issues in the newborn.
Benefits of Taking the Test
Taking the Chromosome Analysis High Resolution Neonatal Test offers numerous benefits:
- Early detection of genetic disorders, enabling timely interventions.
- Peace of mind for parents regarding their child’s health.
- Informed decision-making regarding future medical care and interventions.
- Access to genetic counseling and support services if needed.
Understanding Your Results
Results from the Chromosome Analysis High Resolution Neonatal Test will typically be available within 21 working days. It is important to discuss the results with a healthcare professional who can provide guidance on the implications of any findings. Understanding your results is crucial for planning further medical care or interventions.
Test Details and Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| Chromosome Analysis High Resolution Neonatal Test | 8658 KSh | 9620 KSh |
Sample Collection and Instructions
The test requires a sample of 4 ml (2 ml minimum) of whole blood collected in a green top (Sodium Heparin) tube. Samples should be shipped refrigerated immediately and must not be frozen. The test is recommended between 18-20 weeks of gestation, and a duly filled Chromosome & FISH Analysis Requisition form (Form 17) is mandatory.
Book Your Test Today!
We have branches across Kenya, making it convenient for you to access our services. To book the Chromosome Analysis High Resolution Neonatal Test, please call or WhatsApp us at +254711564616. Early detection can make a significant difference in your child’s health!
