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- Genetics
Genetics
Genetic testing involves the analysis of genetic material. It allows for the identification of genes, the analysis of their functions, and the predisposition to certain diseases or hereditary traits. These tests enable the diagnosis and treatment of many genetic diseases (including cancers) and the assessment of the risk of their occurrence in patients and their offspring.

Diagnostics of cystic fibrosis and other CFTR-related diseases, stage I - analysis of the CFTR gene sequence - exons 4, 8, 11, 12, 14, 20, 23 and 24 (16 most common mutations in the Polish p
The most common mutation, called delta F508, is a deletion of one amino acid at position 508 in the CFTR protein.

Qualification for the EndoRNA test
The EndoRNA test is an innovative test that allows you to quickly diagnose endometriosis. A gynaecologist can qualify you for the EndoRNA test with the possibility of performing the test during one visit. There is a short waiting time for results – about 2-3 weeks.

NeoThetis
A genetic test to select the most optimal method of cancer treatment, known as a liquid biopsy.

Toxocara canis IgG antibodies
Toxocariasis (Toxocara canis) IgG. Serological diagnosis of toxocariasis. Determination of serum levels of IgG antibodies specific for T. canis antigensó

Gluten F79
Gluten is a fraction of plant-derived proteins, consisting of glutenin and, depending on the type of grain, gliadin (wheat), hordein (barley) or secalin (rye).

Genetic panels for hereditary cancers Predict&Prevent - 138 genes
Comprehensive panel to assess predisposition to cancers of multiple organs due to genetic causes. The panel includes 54 genes. The test requires a blood sample.

Analysis of the (TA)n-repeats region in the UGT1A1 gene promoter (c.-55_-54insTA mutation) - diagnostics of Gilbert's syndrome
Gilbert's syndrome is a common genetic disorder and belongs to the fluke of congenital jaundice with a mild course.

Diagnostics of cystic fibrosis and other CFTR-related diseases - analysis of the p.Phe508del mutation of the CFTR gene and over 80 other mutations in exon 11
Analysis of p.Phe508del mutations in the CFTR gene and other mutations in the exon 11

Test on genetic predisposition for hemochromatosis (5 HFE gene mutations)
The test allows the determination of mutations within a gene that determines carrier or disease occurrence: H63D, C282Y, S65C, E168X and Q283P.

Assessment of genetic predisposition to estrogen-dependent cancer/HTGR/(BRCA1- 3 mutations) + (CHEK2-1 mutation)
Diagnosis of genetic predisposition to estrogen-dependent cancer /HTGR/ (BRCA1- 3 mutations) + (CHEK2-1 mutation)