SCA12 Spinocerebellar Ataxia PPP2R2B Gene Mutation Test
Introduction
The SCA12 Spinocerebellar Ataxia PPP2R2B Gene Mutation Test is a vital diagnostic tool for identifying genetic mutations associated with spinocerebellar ataxia, a neurological disorder that affects coordination and balance. Understanding genetic predispositions can significantly impact patient management and treatment options.
What the Test Measures
This test specifically measures mutations in the PPP2R2B gene, which have been linked to the development of spinocerebellar ataxia type 12. By analyzing the genetic code, healthcare providers can determine if a patient carries the mutation that may lead to this condition.
Who Should Consider This Test?
Individuals who should consider the SCA12 test include:
- Those with a family history of spinocerebellar ataxia or other neurological disorders.
- Patients exhibiting symptoms such as unsteady gait, difficulty with fine motor tasks, or coordination problems.
- Individuals concerned about their genetic risk factors related to ataxia.
Benefits of Taking the Test
Taking the SCA12 test offers several benefits:
- Early Diagnosis: Identifying genetic mutations can lead to earlier interventions and management strategies.
- Informed Decision-Making: Understanding genetic risks allows patients and families to make informed choices regarding their health and lifestyle.
- Personalized Treatment: Results can help healthcare providers tailor treatment plans specific to the patient’s genetic profile.
Understanding Your Results
Once the test is completed, results will indicate whether a mutation in the PPP2R2B gene is present. It is essential to discuss these results with a healthcare professional, preferably a neurologist, who can provide guidance on the implications and next steps.
Test Name and Price
| Test Name | Discount Price | Regular Price |
|---|---|---|
| SCA12 Spinocerebellar Ataxia PPP2R2B Gene Mutation Test | 80,000 NGN | 150,000 NGN |
Book Your Test Today
To schedule your SCA12 Spinocerebellar Ataxia PPP2R2B Gene Mutation Test, please contact us at +2348077798758 or visit our website to book online. Take control of your health and gain valuable insights into your genetic predisposition to ataxia.
Test Details
Turnaround Time: 10-12 days
Sample Type: 4 mL (2 mL min.) whole blood in 1 Lavender top (EDTA) tube. Ship refrigerated. DO NOT FREEZE. Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.
Method: PCR, Fragment Analysis
Department: Molecular Diagnostics
Specialty: Neurologist
Disease Type: Neurologic Disorder-Ataxia
Pre-Test Instructions: Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.
