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Medical Information Services Telephone +32 2 714 17 11 Or mail requests to: 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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