Mitochondrial Mutation Detection Comprehensive Panel Test
Introduction
The Mitochondrial Mutation Detection Comprehensive Panel Test is a cutting-edge diagnostic tool designed to identify specific genetic mutations within mitochondrial DNA. Mitochondrial DNA mutations can lead to a variety of neurological disorders and genetic diseases, making this test crucial for early diagnosis and management. By utilizing advanced PCR and sequencing methods, this test offers comprehensive insights into an individual’s genetic makeup, allowing healthcare providers to tailor treatment plans effectively.
What the Test Measures
This test detects mutations in critical mitochondrial genes including:
- ND1
- ND4
- ND5
- ND6
- TL1
- MCTYB1
- ATP6
- ATP8
These genes are essential for mitochondrial function and energy production, and mutations can lead to severe health issues.
Who Should Consider This Test?
This test is recommended for individuals experiencing symptoms associated with:
- Neurological disorders (e.g., muscle weakness, seizures, cognitive decline)
- Genetic diseases with a familial history of mitochondrial dysfunction
Consultation with a neurologist or pediatrician is advisable for those who may be at risk.
Benefits of Taking the Test
- Early detection of mitochondrial mutations can facilitate timely intervention.
- Helps in understanding the genetic basis of neurological symptoms.
- Guides treatment options and management strategies for affected individuals.
- Provides reassurance for families with a history of genetic disorders.
Understanding Your Results
Results from the Mitochondrial Mutation Detection Comprehensive Panel Test will indicate the presence or absence of specific mitochondrial mutations. A healthcare provider will interpret the results and discuss their implications for health and treatment options.
Test Pricing
| Price Type | Amount (KSh) |
|---|---|
| Discount Price | 60,000 |
| Regular Price | 90,000 |
Sample Collection and Pre-Test Instructions
Sample type: 4 mL (2 mL min.) whole blood in 1 Lavender top (EDTA) tube. Ship refrigerated. DO NOT FREEZE. A duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory for processing.
Convenience Across Kenya
We have branches across all major cities in Kenya and offer a home sample collection service for your convenience. To book the Mitochondrial Mutation Detection Comprehensive Panel Test, please call or WhatsApp us at +254746849631.
Book your test today to take a proactive step towards understanding your health!
