Web: | mayocliniclabs.com |
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Email: | mcl@mayo.edu |
Telephone: | 800-533-1710 |
International: | +1 855-379-3115 |
Values are valid only on day of printing. |
See Lysosomal Storage Disorders Diagnostic Algorithm, Part 1 in Special Instructions.
Careful review of clinical findings will help distinguish between GM1 gangliosidosis and Morquio syndrome type B. A diagnosis of galactosialidosis must be additionally demonstrated by a deficiency of neuraminidase (NEURF / Neuraminidase, Fibroblasts).
Provide a reason for referral with each specimen.
Container/Tube:
Preferred: Lavender top (EDTA)
Acceptable: Yellow top (ACD)
Specimen Volume: 2 mL
1. New York Clients-Informed consent is required. Document on the request form or electronic order that a copy is on file. The following documents are available in Special Instructions:
-Informed Consent for Genetic Testing (T576)
-Informed Consent for Genetic Testing-Spanish (T826)
2. Biochemical Genetics Patient Information (T602) in Special Instructions.
3. If not ordering electronically, complete, print, and send an Inborn Errors of Metabolism Test Request (T798) with the specimen.
Specimen Type | Temperature | Time | Special Container |
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Whole blood | Ambient (preferred) | 7 days | |
Refrigerated | 7 days |