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Huntington Disease (HTT gene, detection of expanded CAG triplet-repeat)(CGC genetics)
SKU: MD-NLM626 Categories: , , , , , , , , , , Tags: , , , , , , ,

In Stock

Huntington Disease (HTT gene, detection of expanded CAG triplet-repeat)(CGC genetics)

฿37,760.00

Additional information

Also Known As

Huntington's Genetic Test, HTT Gene Testing
Specimen

EDTA whole blood 3 ml
Turnaround Time

37 days
Test Code

MD-NLM626
Test Type

Special
Related Tests

Genetic Counseling, Neurological Testing

A genetic test that detects expansions of the CAG triplet repeat in the HTT gene, which is responsible for Huntington's disease. Early diagnosis is crucial for family planning and managing symptoms.

Product tags: Depression, Genetic Disorders, HTT Gene Testing, Huntington's Disease, Huntington's Genetic Test, Involuntary Movements, Memory Loss, None
Diseases: Genetic Disorders, Huntington's Disease
Symptoms: Depression, Involuntary Movements, Memory Loss
Habits: None
Age Groups: Adults
Specimens: EDTA Whole Blood
Diagnostic Methods: Fragment Analysis, PCR
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Description

A genetic test that detects expansions of the CAG triplet repeat in the HTT gene, which is responsible for Huntington's disease. Early diagnosis is crucial for family planning and managing symptoms.

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

Huntington's Genetic Test, HTT Gene Testing
Specimen

EDTA whole blood 3 ml
Turnaround Time

37 days
Test Code

MD-NLM626
Test Type

Special
Related Tests

Genetic Counseling, Neurological Testing

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