Detects mitochondrial DNA mutations linked to Kearns-Sayre syndrome and chronic progressive external ophthalmoplegia…. This lab test includes home sample collection via a provided kit or by a clinician, and you’ll receive a comprehensive physical health report with your results.
DNA Mitochondria Mutation for KSS/CPEO
11,025 THB
SKU :
MD-NLB120
Detects mitochondrial DNA mutations linked to Kearns-Sayre syndrome and chronic progressive external ophthalmoplegia.
Lab Categories : All Ages, Blood, Family History, Genetic Disorders, Lab Test, Muscle Weakness, PCR, Vision Problems
Diseases : Genetic Disorders
Symptoms : Muscle Weakness, Vision Problems
Habits : Family History
Age Groups : All Ages
Specimens : Blood
Diagnostic Methods : PCR
| Also Known As | Kearns-Sayre Syndrome DNA Test |
|---|---|
| Specimen | EDTA Whole blood 5 ml |
| Turnaround Time | 4 weeks |
| Test Code | MD-NLB120 |
| Test Type | Special |
| Related Tests | Neurology Panel |
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