MERRF Myoclonic Epilepsy Associated With Ragged Red Fibres Mutation Detection Test
Introduction
The MERRF Myoclonic Epilepsy Associated With Ragged Red Fibres Mutation Detection Test is a vital diagnostic tool used to identify genetic mutations linked to Myoclonic Epilepsy with Ragged Red Fibres (MERRF) syndrome. This rare mitochondrial disorder primarily affects the nervous system and muscle function, leading to a range of debilitating symptoms. Understanding your genetic predisposition through this test can significantly impact your treatment plan and overall quality of life.
What the Test Measures
This test detects specific mutations in mitochondrial DNA that are responsible for MERRF syndrome. By analyzing the genetic material in your blood sample, healthcare professionals can confirm or rule out the presence of these mutations.
Who Should Consider This Test
Individuals experiencing symptoms such as myoclonic seizures, muscle weakness, and ataxia should consider this test. Additionally, those with a family history of mitochondrial disorders or unexplained neurological symptoms may benefit from undergoing this evaluation.
Benefits of Taking the Test
- Accurate diagnosis of MERRF syndrome.
- Informed decision-making regarding treatment options.
- Better understanding of the condition and its implications.
- Potential for personalized healthcare strategies.
Understanding Your Results
Upon receiving your test results, it is essential to discuss them with a qualified neurologist. They will help interpret the findings, explain their significance, and outline possible next steps based on your specific situation.
Test Pricing
Test Name | Discount Price | Regular Price |
---|---|---|
MERRF Myoclonic Epilepsy Associated With Ragged Red Fibres Mutation Detection Test | 320000 NGN | 500000 NGN |
Book Your Test Today!
Don’t wait to understand your neurological health. To book the MERRF Myoclonic Epilepsy Associated With Ragged Red Fibres Mutation Detection Test, contact us at +2348077798758 via call or WhatsApp. Our team is ready to assist you in taking this important step towards better health.
Test Details
- Turnaround Time: Sample Daily by 11 am; Report in 10 days
- Sample Type: 4 mL (2 mL min.) whole blood in 1 Lavender top (EDTA) tube. Ship refrigerated. DO NOT FREEZE.
- Pre-Test Instructions: Duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.
- Specialty: Neurologist
- Department: Molecular Diagnostics
- Method: PCR
- Disease Type: Disorders of Nervous System