SCA23 Spinocerebellar Ataxia PDYN Gene Mutation Test
Introduction
The SCA23 Spinocerebellar Ataxia PDYN Gene Mutation Test is a diagnostic tool used to identify mutations in the PDYN gene, which are associated with spinocerebellar ataxia, a group of neurodegenerative disorders characterized by progressive loss of coordination and balance. This test is vital for patients exhibiting symptoms of ataxia, allowing for early diagnosis and management of the condition.
What the Test Measures
This test specifically detects mutations in the PDYN gene, which plays a crucial role in the functioning of the nervous system. By analyzing the genetic material from a blood sample, healthcare providers can determine if a patient has inherited mutations that may lead to spinocerebellar ataxia.
Who Should Consider This Test
Individuals experiencing symptoms such as:
- Loss of coordination
- Unsteady gait
- Difficulty with fine motor tasks
- Family history of ataxia or related neurological disorders
should consider undergoing this test. Additionally, those with risk factors for neurological disorders may benefit from genetic counseling and testing.
Benefits of Taking the Test
- Early diagnosis of spinocerebellar ataxia, allowing for timely intervention.
- Informs treatment options and management strategies tailored to the individual’s genetic profile.
- Provides valuable information for family members regarding genetic risks.
- Facilitates participation in clinical trials or research studies.
Understanding Your Results
Results from the SCA23 Spinocerebellar Ataxia PDYN Gene Mutation Test will indicate whether mutations in the PDYN gene are present. A positive result suggests a higher likelihood of developing ataxia, while a negative result may provide reassurance. It is essential to discuss your results with a healthcare provider for a comprehensive understanding and appropriate next steps.
Test Pricing
| Price Type | Amount (NGN) |
|---|---|
| Discount Price | 150,000 NGN |
| Regular Price | 300,000 NGN |
Booking the Test
To book the SCA23 Spinocerebellar Ataxia PDYN Gene Mutation Test, please contact us at +2348077798758 via call or WhatsApp. Ensure you provide a duly filled Genomics Clinical Information Requisition Form (Form 20) as it is mandatory for the test.
Test Details
- Sample Type: 4 mL (2 mL min.) whole blood in 1 Lavender top (EDTA) tube. Ship refrigerated. DO NOT FREEZE.
- Turnaround Time: Sample must be submitted by Tuesday 11 am; report will be available on Saturday.
- Department: Molecular Diagnostics
- Method: PCR, Sequencing
- Specialty: Neurologist
- Disease Type: Neurologic Disorder – Ataxia
Take charge of your health today by understanding your genetic predisposition to neurological disorders. Book your SCA23 Spinocerebellar Ataxia PDYN Gene Mutation Test now!
