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DNA Mitochondria Mutation for KSS/CPEO
SKU: MD-NLB120 Categories: , , , , , , , Tags: , , , ,

In Stock

DNA Mitochondria Mutation for KSS/CPEO

฿11,025.00

Additional information

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

Detects mitochondrial DNA mutations linked to Kearns-Sayre syndrome and chronic progressive external ophthalmoplegia.

Product tags: Family History, Genetic Disorders, Kearns-Sayre Syndrome DNA Test, Muscle Weakness, Vision Problems
Diseases: Genetic Disorders
Symptoms: Muscle Weakness, Vision Problems
Habits: Family History
Age Groups: All Ages
Specimens: Blood
Diagnostic Methods: PCR
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Description

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.

Additional information

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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