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  • Mucopolysaccharidosis type I (MPS I) marker

Mucopolysaccharidosis type I (MPS I) marker

Mucopolysaccharidosis type I (MPS I) marker
Test code: GED1D
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Test code: GED1D
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Mucopolysaccharidosis type I (MPS I) marker

This assay detects Mucopolysaccharidosis I (MPS I) biomarker.

View test information
Test Code GED1D
Test Summary

This assay detects Mucopolysaccharidosis I (MPS I) biomarker.

Turn Around Time 7 days
Acceptable Sample Types Dried Blood Spots
Acceptable Billing Types Institutional Billing
NY Approved No
Institutional Price $499.00
*TAT starts after the sample and all required sample information is received at the processing laboratory.

This testing service has not been cleared or approved by the U.S. Food and Drug Administration. Testing services may not be licensed in accordance with the laws in all countries. The availability of specific test offerings is dependent upon laboratory location.
Test code: GED1D
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Test information

  • Test description
  • Indications for testing
  • Condition description
  • Test methods and limitations
  • Detailed sample requirements

Test description

This assay provides a semi-quantitative measurement of a glycosaminoglycan fragment that is specific to Mucopolysaccharidosis I (MPS I).

References:

Saville et al. Genetics in Medicine 2019; 21(3):753-757.
Herbst et al. International Journal of Neonatal Screening 2020; 6(3):69.

Indications for testing

Alpha-L-iduronidase activity is below the normal reference range.

Condition description

Mucopolysaccharidosis type I (MPS I) is a rare autosomal recessive genetic disorder, caused by deficiency of the enzyme alpha-L-iduronidase, resulting in the accumulation of the glycosaminoglycans (GAGs) in organs and tissues (PMID: 32764324).

Test methods and limitations

LC-MS/MS

Limitations:

The effect of anticoagulants on this assay has not been determined, therefore dried blood spots prepared from venous drawn whole blood tubes cannot be accepted.

Detailed sample requirements

Dried Blood Spots
Test Details Page
Collection Container(s)

Dried blood spot card

Collection

Follow kit instructions. Briefly, allow blood to saturate the card until indicated areas are filled and blood has soaked through the card. Air dry the card at ambient temperature for at least 3 hours.

  • NBS: Please contact Revvity Omics to request the StepOne® kit.
  • Gene Sequencing: Please contact Revvity Omics to request the DBS collection kit.
  • For pre-punched DBS: The required minimum is 6 punches
Sample Condition

Follow the instructions provided with the collection set. Store the dried blood at ambient temperature for up to two days. If the specimen cannot be sent as soon as it is dry, the filter paper should be placed in a sealable plastic bag and stored in a refrigerator (≤ 8°C) or preferably in a freezer.

Shipping

Follow kit instructions. Double bag and ship overnight at ambient temperature.

How To Order

Step 1
Choose Your Test

Select the correct test for your patient, and download and fill out the Clinical Genomics test requisition form.

Step 2
Collect Sample

Obtain a sample for testing from the patient using one of the provided Revvity Omics test packs.
 

Step 3
Send Samples

Send samples and all required forms back to Revvity for processing using pre-paid shipping label.

Learn More

1. Build Your Custom Panel

Complete the Genomics Gene Tool Form, and a unique test code will be generated for you.

 

2. Complete and print the test requisition

Complete & print the test requisition.

Ensure that:

  • You entered your unique test code from the Genomics Gene Tool
  • All sections are complete
  • Your patient has signed an informed consent
     

3. Collect and Send Patient Sample

Collect patient sample.

  1. Obtain a sample for testing from the patient and confirm that the sample is correctly labeled with the patient's name and date of birth.
  2. Note: if you do not have a Revvity Omics kit available in your office, please email or call us at 1-866-354-2910.

Send patient sample.

Ship your test kit back using the pre-paid shipping label. Remember to include:

✔   Patient sample

✔   Completed informed consent

✔   Test requisition form

✔   Any applicable medical records or clinical notes
 

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