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Oculopharyngeal muscular dystrophy
SKU: MD-NLMA366 Categories: , , , , , , , Tags: , , , ,

In Stock

Oculopharyngeal muscular dystrophy

฿7,770.00

Additional information

Also Known As

OPMD Genetic Test
Specimen

EDTA whole blood 10 ml
Turnaround Time

2 months
Test Code

MD-NLMA366
Test Type

Special
Related Tests

Genetic Panel

Detects mutations associated with oculopharyngeal muscular dystrophy.

Product tags: Difficulty Swallowing, Drooping Eyelids, Family History, Genetic Disorders, OPMD Genetic Test
Diseases: Genetic Disorders
Symptoms: Difficulty Swallowing, Drooping Eyelids
Habits: Family History
Age Groups: All Ages
Specimens: Blood
Diagnostic Methods: DNA Sequencing, PCR
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Description

Detects mutations associated with oculopharyngeal muscular dystrophy.

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

OPMD Genetic Test
Specimen

EDTA whole blood 10 ml
Turnaround Time

2 months
Test Code

MD-NLMA366
Test Type

Special
Related Tests

Genetic Panel

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