| EX1529 MUCOPOLYSACCHARIDOSIS (MPS) SCREEN, URINE |
| Specimen: |
10 ml (5 ml min.) aliquot of first-morning urine in a sterile screw-capped container. Do not use any preservatives. Ship refrigerated or frozen. Provide brief clinical and drug history. |
| Stability: |
| Room |
Refrigerated |
Frozen |
| 2 hrs |
1 week |
2 weeks |
|
| Method: |
Toluidine blue spot test |
| Comment: |
|
| Report: |
Contact us to know the TAT. |
| Usage: |
Mucopolysaccharidosis (MPS) is an autosomal recessive lysosomal storage disorder. It is due to the deficiency of the enzyme responsible for the catabolism of glycosaminoglycans (GAG). These patients first present with increased urinary GAG excretion. |
| Doctor Specialty: |
Pediatrician |
| Disease: |
Inborn errors of metabolism |
| Components: |
|
| Courier Charges: |
0.00 |
| Home Collection: |
Available (*T&C Apply) |
| Department: |
GENETICS |
| Pre Test Information: |
First-morning urine sample required. Provide brief clinical and drug history. |
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