Leigh Syndrome Mitochondrial Mutation Detection Test
Introduction to the Test
The Leigh Syndrome Mitochondrial Mutation Detection Test is a vital diagnostic tool used to identify genetic mutations associated with Leigh syndrome, a serious neurological disorder that primarily affects the central nervous system. This test is essential for individuals displaying symptoms of mitochondrial dysfunction, enabling early diagnosis and intervention.
What the Test Measures
This test detects specific mutations in mitochondrial DNA that are linked to Leigh syndrome. By analyzing the genetic material, healthcare professionals can determine the presence of mutations that may contribute to the development of this debilitating condition.
Who Should Consider This Test?
Individuals who should consider the Leigh Syndrome Mitochondrial Mutation Detection Test include:
- Patients exhibiting symptoms such as developmental delays, loss of motor skills, and neurological impairments.
- Individuals with a family history of Leigh syndrome or other mitochondrial disorders.
- Patients experiencing unexplained neurological symptoms that may suggest mitochondrial dysfunction.
Benefits of Taking the Test
Taking the Leigh Syndrome Mitochondrial Mutation Detection Test offers several benefits:
- Early diagnosis of Leigh syndrome can lead to timely medical interventions.
- Understanding genetic predispositions can aid in family planning and management of the condition.
- Provides critical information for personalized treatment plans and support.
Understanding Your Results
Results from the Leigh Syndrome Mitochondrial Mutation Detection Test will be interpreted by a qualified healthcare professional. They will explain the significance of any detected mutations and discuss potential next steps in management and treatment.
Test Pricing
| Test Name | Discount Price | Regular Price |
|---|---|---|
| Leigh Syndrome Mitochondrial Mutation Detection Test | 150,000 NGN | 240,000 NGN |
How to Book the Test
To book the Leigh Syndrome Mitochondrial Mutation Detection Test, please contact us at DNA Labs Nigeria. Call or WhatsApp us at +2348077798758 to schedule your appointment and receive further instructions.
Test Details
Turnaround Time: Sample must be submitted by Monday 9 am; report available by Friday.
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.
Pre-Test Instructions: A duly filled Genomics Clinical Information Requisition Form (Form 20) is mandatory.
Specialty: Neurology
Department: Molecular Diagnostics
Method: PCR, Sequencing
Disease Type: Disorders of Nervous System
