N ACETYLGLUCOSAMINE 6 SULPHATASE, HEPARIN BLOOD

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NABL Cap Accredited    
This test measures the activity level of the enzyme N-Acetylglucosamine-6-sulfatase, which plays a key role in breaking down specific complex carbohydrates in the body. Deficiency of this enzyme is associated with Mucopolysaccharidosis type IIID (Sanfilippo syndrome D), a rare inherited metabolic disorder that causes neurological decline. Early diagnosis helps in understanding disease progression, planning appropriate management, and offering genetic counseling. Metropolis Healthcare performs this test using Heparin whole blood with advanced laboratory technology

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Price: Rs. 8,925.00

Sample Type: Sodium Heparin Blood

Fasting Not Required


Notes: N0001

Frequently Asked Questions (FAQ's):

What does the N-Acetylglucosamine-6-Sulfatase test help diagnose?
This test helps diagnose Mucopolysaccharidosis type IIID, a rare lysosomal storage disorder affecting neurological function.

How does Metropolis Healthcare perform this test?
Metropolis Healthcare uses specialized biochemical enzyme assays on Heparin blood to accurately measure enzyme activity levels.

Who should undergo this test?
Individuals with symptoms such as developmental delay, behavioral issues, hearing loss, or suspicion of MPS disorders may require this test.

What sample is required for this test?
Heparinized whole blood is needed for enzyme analysis.

Is fasting required before sample collection?
No fasting is required for this test.

How long does Metropolis Healthcare take to provide results?
Reporting time may vary due to test complexity; Metropolis Healthcare shares results within the standard turnaround schedule.

Does this test require genetic counseling?
Yes, genetic counseling is recommended for families with confirmed or suspected enzyme deficiency.

Can this test help support treatment planning?
Yes, results assist clinicians in determining supportive therapies, follow-up tests, and family screening options at Metropolis Healthcare.

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