RB1 Gene Hereditary Retinoblastoma NGS Genetic DNA Test
Introduction to the Test
The RB1 Gene Hereditary Retinoblastoma NGS Genetic DNA Test is a specialized genetic test designed to identify mutations in the RB1 gene, which are associated with hereditary retinoblastoma, a rare but serious eye cancer that primarily affects children. Understanding the genetic basis of this condition is essential for early diagnosis, treatment, and family planning.
What the Test Measures
This test utilizes Next Generation Sequencing (NGS) technology to detect specific mutations in the RB1 gene. By analyzing the genetic material, healthcare providers can determine whether a child is at risk of developing retinoblastoma.
Who Should Consider This Test?
Parents or guardians of children who exhibit symptoms such as:
- Leukocoria (white pupil)
- Strabismus (crossed eyes)
- Vision impairment
Additionally, individuals with a family history of retinoblastoma or those who have relatives affected by the disease should consider this test.
Benefits of Taking the Test
- Early detection of hereditary retinoblastoma.
- Informed decision-making regarding treatment options.
- Guidance for family planning and genetic counseling.
- Peace of mind for families at risk.
Understanding Your Results
Results from the RB1 Gene Hereditary Retinoblastoma NGS Genetic DNA Test will help determine the presence of mutations in the RB1 gene. A genetic counselor will assist in interpreting these results, providing insights into the implications for the patient and their family.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
How to Book the Test
To book the RB1 Gene Hereditary Retinoblastoma NGS Genetic DNA Test, please contact us at +2348077798758 or visit our website. Our team is ready to assist you with scheduling and any inquiries you may have.
Additional Information
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
Pre-Test Instructions: A clinical history of the patient is required, along with a genetic counseling session to draw a pedigree chart of family members affected by the RB1 gene.
Our dedicated team of ophthalmologists and genetic specialists is committed to providing you with the highest quality care and support throughout the testing process.
