Mucopolysaccharidosis VI

Mucopolysaccharidosis VI, also known as Maroteaux-Lamy syndrome, is a rare disease characterised by progressive enlargement of many tissues, that can also become inflamed or scarred, and eventually waste away (atrophy). It is associated with a deficiency of arylsulfatase B (ASB) leading to the accumulation of dermatan sulfate.

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Antigen
Molecular Class
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CoA
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Expiry Date
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Enzyme
Naglazyme®
1,0 mg/mL
0,2 mg
2-8°C / -80°C
07/2023
646,00 
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