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GILBERT SYNDROME

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1 200 Kč

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A genetic blood test for Gilbert's syndrome identifies mutations in the UGT1A1 gene. This mutation leads to reduced activity of the enzyme that processes bilirubin in the liver, resulting in elevated bilirubin levels in the blood, which may cause jaundice.

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A genetic blood test for Gilbert's syndrome identifies mutations in the UGT1A1 gene. This mutation leads to reduced activity of the enzyme that processes bilirubin in the liver, resulting in elevated bilirubin levels in the blood, which may cause jaundice. Gilbert's syndrome is a benign condition that typically does not require treatment.