SLC16A2 Gene Allan-Herndon-Dudley Syndrome NGS Genetic DNA Test
The SLC16A2 Gene Allan-Herndon-Dudley Syndrome NGS Genetic DNA Test is a cutting-edge diagnostic tool that utilizes Next-Generation Sequencing (NGS) technology to analyze genetic variations associated with Allan-Herndon-Dudley syndrome, a rare neurological disorder. This test plays a crucial role in identifying genetic anomalies that may lead to cognitive impairments and motor dysfunctions, allowing for timely interventions and management strategies.
What the Test Measures
This genetic test specifically measures variations in the SLC16A2 gene, which is responsible for the transport of thyroid hormones into the brain. Abnormalities in this gene can result in significant neurological complications. By detecting these genetic changes, healthcare providers can better understand the underlying causes of neurological symptoms in patients.
Who Should Consider This Test?
Patients exhibiting symptoms such as developmental delays, cognitive impairments, or motor skill deficiencies should consider this test. Additionally, individuals with a family history of Allan-Herndon-Dudley syndrome or related neurological disorders may benefit from genetic testing to assess their risk and inform treatment options.
Benefits of Taking the Test
- Early identification of genetic predispositions to Allan-Herndon-Dudley syndrome.
- Informed decision-making regarding treatment and management strategies.
- Access to genetic counseling and support for affected families.
- Improved understanding of the neurological disorder and its implications.
Understanding Your Results
Results from the SLC16A2 Gene Allan-Herndon-Dudley Syndrome NGS Genetic DNA Test will be provided in a comprehensive report. It is essential to discuss these results with a qualified healthcare provider or genetic counselor to understand their implications fully. They can guide you through the findings and recommend appropriate next steps based on your results.
Test Pricing
Test Name | Discount Price | Regular Price |
---|---|---|
SLC16A2 Gene Allan-Herndon-Dudley Syndrome NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Turnaround time for results is approximately 3 to 4 weeks. The sample type required for this test can be blood, extracted DNA, or one drop of blood on an FTA card.
Before undergoing the test, patients are advised to have a clinical history assessment and a genetic counseling session to draw a pedigree chart of family members affected by the SLC16A2 Gene Allan-Herndon-Dudley syndrome.
Book Your Test Today!
Don’t wait to gain insights into your genetic health. Book the SLC16A2 Gene Allan-Herndon-Dudley Syndrome NGS Genetic DNA Test today by calling or sending a WhatsApp message to +2348110567037. Your health is important, and early diagnosis can make a significant difference!