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Gilbert syndrome is a hereditary disorder associated with a defect in the UGT (glucuronyltransferase) gene, which is involved in bilirubin* metabolism in the body. This leads to an increase in bilirubin in the blood (usually not more than 80-100 µmol/l, with a significant predominance of indirect bilirubin) and to the occasional occurrence of moderate jaundice (yellow staining of the skin, mucous membranes, whites of the eyes). Other biochemical blood parameters and liver tests remain within normal limits.... Read more

Gilbert syndrome is a hereditary disorder associated with a defect in the UGT (glucuronyltransferase) gene, which is involved in bilirubin* metabolism in the body. This leads to an increase in bilirubin in the blood (usually not more than 80-100 µmol/l, with a significant predominance of indirect bilirubin) and to the occasional occurrence of moderate jaundice (yellow staining of the skin, mucous membranes, whites of the eyes). Other biochemical blood parameters and liver tests remain within normal limits.... Read more

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JAK2 gene, VAL617Phe mutation, Qualitative. JAK-2 is a genetic marker associated with pathological activation of division and maturation (differentiation) of myeloid hematopoietic progenitor cells.

IL-33 is a key factor in the development of allergic diseases, including bronchial asthma, allergic rhinitis, and polyposis rhinosinusitis (PRS). Based on the results of genetic analysis, we can predict the course of these pathologies and predict the development of severe forms. The IL-33 gene ANALYSIS is represented by two points: rs1342326 ... Read more

BRCA1, BRCA2, CHEK2 gene analysis BRCA1, BRCA2 and CHEK2 gene analysis will determine your individual risk of getting breast or ovarian cancer during your lifetime. Breast cancer is a multifactorial disease, meaning that its development is related to both environmental ... Read more