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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Product Batch	Antigen	Molecular Class	Drug Brand	Product Concentration	CoA	Quantity per vial	Storage Temperature	Expiry Date	Price from
Galsulfase L062084		Enzyme	Naglazyme®	1,0 mg/mL	–	0,2 mg	2-8°C / -80°C	07/2023	548,00 €	view product Max: 10 Min: 1 Step: 1