Mitochondrial Encephalomyopathy Lactic Acidosis and Strokelike Episodes MELAS Mutation Detection Test
Introduction
The Mitochondrial Encephalomyopathy Lactic Acidosis and Strokelike Episodes (MELAS) Mutation Detection Test is a specialized diagnostic tool designed to identify genetic mutations associated with MELAS, a serious condition that affects the nervous system and other systems in the body. This test is essential for patients displaying symptoms of mitochondrial disorders, providing crucial insights that can guide treatment and management strategies.
What the Test Measures
This test detects specific mutations in mitochondrial DNA that are linked to MELAS. By analyzing the genetic material, healthcare providers can determine the presence of these mutations, which can significantly impact a patient’s health and treatment options.
Who Should Consider This Test?
Individuals who experience symptoms such as:
- Recurrent strokes or stroke-like episodes
- Severe headaches
- Seizures
- Muscle weakness
- Developmental delays
are advised to consider this test. Additionally, those with a family history of mitochondrial diseases or unexplained neurological symptoms should consult their healthcare provider about the MELAS Mutation Detection Test.
Benefits of Taking the Test
- Early diagnosis of MELAS can lead to timely intervention and management.
- Understanding genetic factors can inform treatment options and lifestyle changes.
- Helps in family planning by identifying hereditary risks.
- Provides peace of mind through accurate diagnosis.
Understanding Your Results
Results from the MELAS Mutation Detection Test can indicate the presence or absence of mutations associated with MELAS. It is important to discuss the results with a qualified healthcare provider, who can explain their implications and recommend further steps.
Test Pricing
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| Mitochondrial Encephalomyopathy Lactic Acidosis and Strokelike Episodes MELAS Mutation Detection Test | 150,000 NGN | 220,000 NGN |
Booking Information
To book the Mitochondrial Encephalomyopathy Lactic Acidosis and Strokelike Episodes MELAS Mutation Detection Test, please ensure you have a duly filled Genomics Clinical Information Requisition Form (Form 20) ready. For sample collection, 4 mL (2 mL minimum) of whole blood in a Lavender top (EDTA) tube is required. Ship the sample refrigerated and avoid freezing.
For more information or to schedule your appointment, call or WhatsApp us at +2348077798758.
Turnaround Time
Samples should be submitted by Monday 9 AM, with reports available by Friday.
