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Myotonic Dystrophy Type 2 3q 21

This molecular test identifies CCTG repeat expansion in the CNBP gene associated with Myotonic Dystrophy Type 2. It aids in differentiating DM2 from DM1, confirming diagnosis, and guiding clinical management of muscle weakness, pain, and systemic involvement.

43 days

Report Ready

No Fasting

Fasting

5-99

Age Group

Home

Collection

Preparation

Why this test

Fasting Required

Not Required

⏱ Report Time

43 days

🧫 Sample Type

Blood

🎂 Age Group

5-99

👤 Gender

Male,Female

🏠 Collection

Home Visit

Myotonic Dystrophy Type 2 3q 21

₹22,500

Inclusive of all taxes. Free home collection.

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4.9
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Step 01

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Step 03

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Step 04

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