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Lahalak Medical PlatformDifferentiate Care
UGT1A1 Full Gene Sequencing for Crigler-Najjar Syndrome
Identify the genetic root of chronic high bilirubin levels. This advanced sequencing test accurately diagnoses Crigler-Najjar syndrome and hereditary liver disorders, enabling precise clinical management and informed genetic counseling.
An advanced genetic test analyzing the DNA sequence of the UGT1A1 gene. It is used to diagnose hereditary hyperbilirubinemia and identify genetic mutations causing rare liver conditions.
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