SLC6A3 Gene Parkinsonism-Dystonia Infantile NGS Genetic DNA Test
Introduction
The SLC6A3 Gene Parkinsonism-Dystonia Infantile NGS Genetic DNA Test is an advanced diagnostic tool designed to identify genetic mutations associated with Parkinsonism and dystonia in infants. This test utilizes Next Generation Sequencing (NGS) technology to provide accurate and comprehensive results, playing a crucial role in the early diagnosis and management of neurological disorders.
What the Test Measures
This genetic test specifically measures variations in the SLC6A3 gene, which have been linked to movement disorders such as Parkinsonism and dystonia. By analyzing the DNA, healthcare professionals can determine if a child has inherited genetic predispositions that may lead to these conditions.
Who Should Consider This Test?
Parents and guardians should consider this test if:
- The child exhibits symptoms of movement disorders, such as abnormal muscle tone or difficulty with coordination.
- There is a family history of Parkinsonism or dystonia.
- There are other neurological symptoms present that warrant further investigation.
Benefits of Taking the Test
- Early identification of genetic predispositions can lead to timely interventions and management strategies.
- Understanding the genetic factors can provide families with valuable information for future planning.
- Access to specialized care from neurologists and genetic counselors based on the test results.
Understanding Your Results
Once the test is completed, results will be analyzed and interpreted by qualified healthcare professionals. It is essential to have a follow-up consultation to discuss the implications of the results and any necessary next steps for management or treatment.
Test Details and Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| SLC6A3 Gene Parkinsonism-Dystonia Infantile NGS Genetic DNA Test | 400,000 NGN | 560,000 NGN |
Booking the Test
Ready to take the next step in understanding your child’s health? Book the SLC6A3 Gene Parkinsonism-Dystonia Infantile NGS Genetic DNA Test today. For more information or to schedule an appointment, please call or WhatsApp us at +2348110567037. Our team of experts is here to assist you!
Additional Information
Turnaround time for results is approximately 3 to 4 weeks. The sample required for this test can be blood or extracted DNA, or even a drop of blood on an FTA card. Prior to testing, a clinical history and genetic counseling session are recommended to draw a pedigree chart of family members affected by SLC6A3 Gene Parkinsonism-Dystonia.
Consult with a neurologist or genetic specialist to determine if this test is appropriate for your child’s symptoms and family history.
