KIF1C Gene Spastic Ataxia Type 2 Autosomal Recessive NGS Genetic DNA Test
Introduction
The KIF1C Gene Spastic Ataxia Type 2 Autosomal Recessive NGS Genetic DNA Test is a specialized genetic test designed to identify mutations in the KIF1C gene, which are associated with spastic ataxia type 2, a neurological disorder. This test utilizes Next Generation Sequencing (NGS) technology to provide accurate and comprehensive results.
What the Test Measures
This genetic test detects specific mutations in the KIF1C gene that may lead to the development of spastic ataxia type 2. By analyzing the genetic material from a blood sample or extracted DNA, the test can reveal the presence of pathogenic variants that contribute to this condition.
Who Should Consider This Test
Individuals with a family history of spastic ataxia or those exhibiting symptoms such as unsteady gait, coordination difficulties, and muscle weakness should consider this test. Risk factors may include a known family history of neurological disorders and specific clinical symptoms that suggest a genetic cause.
Benefits of Taking the Test
- Accurate diagnosis of genetic conditions affecting neurological function.
- Informed decision-making regarding family planning and potential health risks.
- Access to tailored treatment options and genetic counseling based on results.
Understanding Your Results
Results from the KIF1C Gene Spastic Ataxia Type 2 test will indicate whether any pathogenic mutations were detected. A genetic counseling session is recommended to interpret these results and discuss implications for the individual and their family.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 400,000 NGN |
| Regular Price | 560,000 NGN |
Booking the Test
To book the KIF1C Gene Spastic Ataxia Type 2 Autosomal Recessive NGS Genetic DNA Test, please contact us at +2348077798758. Our team is ready to assist you with scheduling your test and providing any additional information you may need.
Test Details
- Turnaround Time: 3 to 4 Weeks
- Sample Type: Blood or Extracted DNA or One drop Blood on FTA Card
- Pre-Test Instructions: Clinical history of the patient and a genetic counseling session to draw a pedigree chart of affected family members.
- Specialty: Neurology
- Department: Genetics
- Method: NGS Technology
- Disease Type: Neurological Disorders
