| EX1578 NEWBORN SCREENING PANEL EXTENDED |
| Specimen: |
1 drop of heel prick blood each on 3 spots of filter paper. Ship refrigerated or frozen. Clinical details and drug history must accompany the sample. |
| Stability: |
| Room |
Refrigerated |
Frozen |
| 2 hrs |
1 week |
1 week |
|
| Method: |
TMS, Fluoroimmunoassay |
| Comment: |
|
| Report: |
Contact us to know the TAT. |
| Usage: |
The aim of newborn screening is to detect diagnostic markers of treatable disorders in blood spots collected from pre-symptomatic newborns. Early identification of disorders significantly improves the long-term prognosis of affected patients, minimizes complications, avoids unnecessary diagnostic testing, and identifies families for whom prenatal genetic counseling may be helpful. |
| Doctor Specialty: |
Pediatrician |
| Disease: |
Inborn errors of metabolism |
| Components: |
*Biotinidase *Cystic Fibrosis *G6PD *Galactosemia *17-Hydroxyprogesterone *TSH *Tandem Mass Spectrometry – 30 Disorders |
| Courier Charges: |
0.00 |
| Home Collection: |
Available (*T&C Apply) |
| Department: |
GENETICS |
| Pre Test Information: |
Clinical details and drug history must accompany the sample. |
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