IFRD1 Gene Spinocerebellar Ataxia Type 18 Autosomal Dominant NGS Genetic DNA Test
Introduction
The IFRD1 Gene Spinocerebellar Ataxia Type 18 Autosomal Dominant NGS Genetic DNA Test is a cutting-edge genetic test that assesses the presence of mutations in the IFRD1 gene, which are linked to Spinocerebellar Ataxia Type 18 (SCA18). This condition is a hereditary neurological disorder characterized by progressive loss of coordination and balance, affecting the cerebellum of the brain.
What the Test Measures
This test employs Next-Generation Sequencing (NGS) technology to accurately detect mutations in the IFRD1 gene. By analyzing the genetic material from a blood sample or extracted DNA, healthcare providers can identify potential genetic risks associated with SCA18.
Who Should Consider This Test?
- Individuals with a family history of Spinocerebellar Ataxia Type 18 or other neurological disorders.
- Patients exhibiting symptoms such as unsteady gait, difficulty with fine motor skills, or coordination issues.
- Those seeking genetic counseling to understand their risk of inheriting or passing on genetic conditions.
Benefits of Taking the Test
- Early diagnosis of genetic predispositions allows for timely intervention and management.
- Provides valuable information for family planning and genetic counseling.
- Helps in understanding the risk of developing neurological disorders.
Understanding Your Results
Upon completion of the test, results will be analyzed and interpreted by a qualified genetic counselor or neurologist. It’s essential to discuss your results in detail to understand their implications on your health and family.
Test Name and Price
| Test Name | Discount Price | Regular Price |
|---|---|---|
| IFRD1 Gene Spinocerebellar Ataxia Type 18 Autosomal Dominant NGS Genetic DNA Test | 40,000 KSh | 56,000 KSh |
Branches and Booking
We have branches across Kenya, including major cities like Nairobi, Mombasa, and Kisumu. We also offer a convenient home sample collection service. To book the IFRD1 Gene Spinocerebellar Ataxia Type 18 Autosomal Dominant NGS Genetic DNA Test, please call or WhatsApp us at +254711564616.
Pre-Test Instructions
Prior to taking the test, it is recommended to have a genetic counseling session to draw a pedigree chart of family members affected by the IFRD1 gene mutation. This will aid in understanding the familial implications of the test results.
Take charge of your health today by booking the IFRD1 Gene Spinocerebellar Ataxia Type 18 Autosomal Dominant NGS Genetic DNA Test!
