Detects mutations in the UGT1A1 gene, which cause Crigler-Najjar syndrome, a disorder that affects bilirubin metabolism…. This lab test includes home sample collection via a provided kit or by a clinician, and you’ll receive a comprehensive physical health report with your results.
Criggler-Najjar (UGT1A1)
Detects mutations in the UGT1A1 gene, which cause Crigler-Najjar syndrome, a disorder that affects bilirubin metabolism.
11,875 THB
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Lab Categories : Crigler-Najjar Syndrome, EDTA Whole Blood, High Bilirubin Levels, Jaundice, Lab Test, Liver Disorders, None, PCR and Direct Sequencing, Pediatrics
Diseases : Crigler-Najjar Syndrome, Liver Disorders
Symptoms : High Bilirubin Levels, Jaundice
Habits : None
Age Groups : Pediatrics
Specimens : EDTA Whole Blood
Diagnostic Methods : PCR and Direct Sequencing
| Also Known As | Crigler-Najjar Genetic Test |
|---|---|
| Specimen | EDTA whole blood 6 mL |
| Turnaround Time | 60 days |
| Test Code | MD-NLB049 |
| Test Type | Special |
| Related Tests | Genetic Testing,Liver Function Panel |
