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About Lysosomal Storage Disease
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MPS I
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Medical Information Services

Telephone +32 2 714 17 11
Fax +32 2 714 17 07

Or mail requests to:
Genzyme Belgium
Ikaroslaan 53
1930 Zaventem

For information on obtaining the services listed below, or for other information, contact Genzyme Belgium.

Enzyme Assay Diagnostic Service:

The diagnosis of MPS I disease is confirmed by the assay of the deficient enzyme alpha-L-iduronidase. Blood samples are the most practical way to test enzyme activity in the plasma or leukocytes.

Urinary GAG Testing Service

Clearance of the accumulating substrate GAG can serve as a surrogate marker of treatment response.

Genotyping Service

MPS I disease is an autosomal recessive disorder. DNA analysis can be a valuable tool for investigating family pedigrees.

Contact your local Genzyme representative or e-mail us for a copy of our CD-ROM, which contains MPS I presentations in PowerPoint format.

 
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01/01/2007: Low bone density in Gaucher disease improves with CerezymeŽ

01/05/2007: Treatment for Pompe disease now available for Belgian patients

01/03/2006: Early treatment with FabrazymeŽ significantly slows progression of Fabry

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Lysosomal Storage Disorders
General information
Gaucher Disease
Fabry Disease
MPS I Disease
Pompe Disease