ALDH3A2 Gene Sjogren-Larsson Syndrome NGS Genetic DNA Test
The ALDH3A2 Gene Sjogren-Larsson Syndrome NGS Genetic DNA Test is a specialized genetic test designed to identify mutations in the ALDH3A2 gene, which are associated with Sjogren-Larsson syndrome, a rare neurological disorder. This test employs Next Generation Sequencing (NGS) technology, providing a comprehensive analysis of the gene to aid in the diagnosis and understanding of this condition.
Importance of the Test
Understanding genetic predisposition is crucial for individuals and families affected by Sjogren-Larsson syndrome. This test not only helps in confirming a diagnosis but also plays a significant role in guiding treatment options and management strategies. Early detection can lead to timely interventions that improve the quality of life.
What the Test Measures
The ALDH3A2 gene is responsible for producing an enzyme that is essential for the metabolism of certain fatty acids. Mutations in this gene can lead to the accumulation of toxic substances, resulting in neurological symptoms. The NGS technology used in this test allows for a detailed examination of the gene, identifying any mutations that may be present.
Who Should Consider This Test?
Individuals showing symptoms of Sjogren-Larsson syndrome, such as:
- Neurological impairments
- Visual disturbances
- Skin abnormalities
- Family history of Sjogren-Larsson syndrome
Additionally, those with risk factors or a clinical history suggesting a genetic predisposition may also benefit from this test.
Benefits of Taking the Test
- Accurate diagnosis of Sjogren-Larsson syndrome
- Informed family planning and genetic counseling
- Guidance for treatment and management options
- Understanding the genetic basis of symptoms
Understanding Your Results
Results from the ALDH3A2 Gene Sjogren-Larsson Syndrome NGS Genetic DNA Test will indicate whether any mutations are present in the ALDH3A2 gene. It is essential to consult with a genetic counselor or healthcare provider to interpret the results accurately and discuss the implications for health and family members.
Test Pricing
| Price Type | Price (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
Book the Test
To book the ALDH3A2 Gene Sjogren-Larsson Syndrome NGS Genetic DNA Test, please contact us at +2348077798758 or visit our website. Take the first step towards understanding your genetic health today!
Turnaround Time: 3 to 4 Weeks
Sample Type: Blood
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 with ALDH3A2 Gene Sjogren-Larsson syndrome.
Specialty: Neurology
Department: Genetics
Method: NGS Technology
Disease Type: Neurological Disorders
