SLC25A4 Gene Progressive External Ophthalmoplegia with Mitochondrial Deletions Type 2 Autosomal Dominant NGS Genetic DNA Test
Introduction
The SLC25A4 Gene Progressive External Ophthalmoplegia with Mitochondrial Deletions Type 2 Autosomal Dominant NGS Genetic DNA Test is a vital diagnostic tool for identifying genetic mutations associated with progressive external ophthalmoplegia (PEO). This condition is characterized by muscle weakness and paralysis of the eye muscles, leading to significant visual impairment. Understanding your genetic predisposition can help in early diagnosis and management of this disorder.
What the Test Measures
This genetic test specifically measures alterations in the SLC25A4 gene, which is crucial for mitochondrial function. Mitochondria are the powerhouses of the cell, and any dysfunction can lead to various neurological disorders, including PEO. By analyzing the DNA, the test can detect mutations that may contribute to the development of these conditions.
Who Should Consider This Test
Individuals with a family history of progressive external ophthalmoplegia or other mitochondrial disorders should consider this test. Symptoms to watch for include:
- Weakness in eye muscle control
- Drooping eyelids
- Difficulty in moving the eyes
- Family members diagnosed with mitochondrial disorders
If you experience these symptoms or have risk factors, consulting with a neurologist is advisable.
Benefits of Taking the Test
- Early diagnosis of genetic disorders.
- Informed decision-making regarding treatment options.
- Genetic counseling can guide family planning.
- Understanding the risk of passing on genetic conditions to offspring.
Understanding Your Results
Results from the SLC25A4 Gene test will provide insight into whether you carry mutations associated with progressive external ophthalmoplegia. It is crucial to discuss your results with a healthcare professional who can explain the implications and guide you on the next steps.
Test Pricing
| Discount Price | Regular Price |
|---|---|
| 400,000 NGN | 560,000 NGN |
Book Your Test Today!
Take control of your health by understanding your genetic predispositions. To book the SLC25A4 Gene Progressive External Ophthalmoplegia with Mitochondrial Deletions Type 2 Autosomal Dominant NGS Genetic DNA Test, please call or WhatsApp us at +2348077798758. Our team is ready to assist you in your journey towards better health.
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 affected family members.
For more information, feel free to reach out to our knowledgeable staff at DNA Labs Nigeria.
