Leigh Syndrome Mitochondrial Mutation Detection Test
Introduction
The Leigh Syndrome Mitochondrial Mutation Detection Test is a pivotal diagnostic tool used to identify Leigh syndrome, a rare but severe neurological disorder characterized by progressive loss of mental and movement abilities. This test is essential for understanding the underlying genetic factors that contribute to this condition, enabling healthcare professionals to make informed decisions regarding patient care.
What the Test Measures
This test specifically measures mitochondrial mutations that are implicated in Leigh syndrome. Mitochondria are the powerhouses of cells, and any mutations can disrupt energy production, leading to significant neurological impairment.
Who Should Consider This Test
Individuals who exhibit symptoms such as developmental delays, loss of motor skills, seizures, and other neurological issues should consider this test. Additionally, those with a family history of Leigh syndrome or other mitochondrial disorders may benefit from testing, as early diagnosis can significantly impact treatment and management.
Benefits of Taking the Test
- Early diagnosis of Leigh syndrome allows for timely intervention and management.
- Understanding genetic predispositions can help in familial planning.
- Facilitates tailored treatment options based on specific mitochondrial mutations.
- Provides peace of mind for families regarding genetic concerns.
Understanding Your Results
Results from the Leigh Syndrome Mitochondrial Mutation Detection Test will indicate the presence or absence of specific mitochondrial mutations. It is essential to discuss these results with a healthcare provider who can provide guidance on the implications and next steps based on the findings.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| Leigh Syndrome Mitochondrial Mutation Detection Test | 15,000 KSh | 24,000 KSh |
Sample Collection Instructions
For this test, a sample of 4 mL (2 mL min.) whole blood must be collected in a lavender top (EDTA) tube. The sample should be shipped refrigerated and must not be frozen. A duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory for processing.
Turnaround Time
Samples must be submitted by Monday 9 am, with results reported by Friday.
Branches Across Kenya
We have branches in all major cities across Kenya, ensuring easy access to our services. For your convenience, we also offer home sample collection services.
Book the Test Today!
Don’t wait to get the answers you need. Book the Leigh Syndrome Mitochondrial Mutation Detection Test today! For inquiries or to schedule an appointment, please call or WhatsApp us at +254711564616.
