GILBERT SYNDROME

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1 600 Kč

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This genetic test identifies mutations in the UGT1A1 gene, which cause Gilbert's syndrome. 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.

The test is performed using a cheek swab (buccal mucosa) - the collection kit will be sent to your address.

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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.