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Mucopolysaccharides (MPS) Type-I

This test evaluates for Mucopolysaccharidosis Type I, a lysosomal storage disorder caused by alpha-L-iduronidase deficiency. It detects accumulation of glycosaminoglycans in biological samples. Early diagnosis is essential for timely initiation of enzyme replacement therapy, disease monitoring, and genetic counseling in affected families.

8 days

Report Ready

No Fasting

Fasting

5-99

Age Group

Home

Collection

Preparation

Why this test

Fasting Required

Not Required

⏱ Report Time

8 days

🧫 Sample Type

Blood

🎂 Age Group

5-99

👤 Gender

Male,Female

🏠 Collection

Home Visit

Mucopolysaccharides (MPS) Type-I

₹12,500

Inclusive of all taxes. Free home collection.

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Step 01

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Step 03

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Step 04

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