SLC24A5 Gene Albinism Oculocutaneous Nonsyndromic NGS Genetic DNA Test
Introduction to the Test
The SLC24A5 Gene Albinism Oculocutaneous Nonsyndromic NGS Genetic DNA Test is a comprehensive genetic analysis designed to detect variations in the SLC24A5 gene, which is associated with oculocutaneous albinism. This test is crucial for understanding the genetic basis of albinism, a condition characterized by a lack of melanin in the skin, hair, and eyes, leading to various visual and dermatological issues.
What the Test Measures
This genetic test specifically measures the presence of mutations in the SLC24A5 gene. By utilizing Next-Generation Sequencing (NGS) technology, it provides a detailed analysis of the genetic material, helping to confirm or rule out a diagnosis of oculocutaneous albinism.
Who Should Consider This Test
This test is recommended for individuals who:
- Have a family history of albinism.
- Exhibit symptoms such as light skin, light hair, and vision problems.
- Are seeking genetic counseling for family planning purposes.
Benefits of Taking the Test
Undergoing the SLC24A5 Gene Albinism test offers numerous benefits:
- Accurate diagnosis of albinism, leading to appropriate management strategies.
- Informed family planning decisions based on genetic risks.
- Access to tailored educational resources and support for affected individuals.
Understanding Your Results
Results from the SLC24A5 Gene Albinism test will indicate whether any mutations were detected in the SLC24A5 gene. A genetic counselor will assist in interpreting the results and discussing the implications for your health and family.
Test Details
| Test Name | Price (NGN) |
|---|---|
| SLC24A5 Gene Albinism Oculocutaneous Nonsyndromic NGS Genetic DNA Test | Discount Price: 400,000 NGN |
| Regular Price: 560,000 NGN |
Booking Your Test
To book the SLC24A5 Gene Albinism Oculocutaneous Nonsyndromic NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you and guide you through the process.
Additional Information
The turnaround time for results is approximately 3 to 4 weeks. The sample type required can be blood or extracted DNA, or even one drop of blood on an FTA card. Prior to the test, a clinical history of the patient is essential, along with a genetic counseling session to create a pedigree chart of family members affected by SLC24A5 gene albinism.
For more details on the SLC24A5 Gene Albinism Oculocutaneous Nonsyndromic NGS Genetic DNA Test, please reach out to our specialists in the Genetics department, particularly for ophthalmology disorders.
