Leigh Syndrome Mitochondrial Encephalopathy Gene Panel
Introduction
The Leigh Syndrome Mitochondrial Encephalopathy Gene Panel is an advanced genetic test designed to identify mutations linked to Leigh syndrome, a serious neurological disorder characterized by progressive loss of mental and movement abilities. This test plays a vital role in early diagnosis and management, providing invaluable insights for affected individuals and their families.
What the Test Measures
This gene panel specifically detects mutations in genes associated with mitochondrial function, which are crucial for cellular energy production. By identifying these mutations, healthcare providers can better understand the underlying causes of Leigh syndrome.
Who Should Consider This Test
Individuals who exhibit symptoms such as developmental delays, loss of motor skills, or neurological deterioration should consider this test. Additionally, family members of diagnosed individuals may benefit from genetic counseling and testing to assess their risk of carrying the mutations.
Benefits of Taking the Test
- Early diagnosis can lead to timely interventions and management strategies.
- Understanding genetic risks can assist in family planning.
- Access to targeted therapies and support resources.
Understanding Your Results
Results from the Leigh Syndrome Mitochondrial Encephalopathy Gene Panel will be interpreted by a qualified healthcare professional. They will provide guidance on the implications of the findings and recommend any necessary follow-up actions.
Test Pricing
| Test Name | Discount Price (NGN) | Regular Price (NGN) |
|---|---|---|
| Leigh Syndrome Mitochondrial Encephalopathy Gene Panel | 720,000 NGN | 960,000 NGN |
Booking Information
The Leigh Syndrome Mitochondrial Encephalopathy Gene Panel can be performed with a Doctor’s prescription. Please note that a prescription is not applicable for surgical cases, pregnancy, or individuals planning to travel abroad. To book your test, please contact us at +2348077798758 or visit our website.
Test Details
- Turnaround Time: 4-6 weeks
- Sample Type: Amniotic fluid / Chorionic villi / Peripheral blood
- Test Components: Sterile container, Sterile Normal Saline Container, EDTA Vacutainer (3 ml)
For further information or to schedule your test, please reach out to us today!
