Thrombophilia (sometimes hypercoagulability or a prothrombotic state) is an abnormality of blood coagulation that increases the risk of thrombosis (blood clots in blood vessels). Such abnormalities can be identified in 50% of people who have an episode of thrombosis (such as deep vein thrombosis in the leg) that was not provoked by other causes. A significant proportion of the population has a detectable abnormality, but most of these only develop thrombosis in the presence of an additional risk factor.
Only for Factor V (R506Q) carriers
Test DetailsThe analysis includes the main panel, ACE ( I/D ) и Factor XIII ( Val34Leu ).
Test DetailsFamilial hypercholesterolemia is an autosomal dominant disorder characterized by elevation of serum cholesterol bound to low density lipoprotein (LDL), which promotes deposition of cholesterol in the skin (xanthelasma), tendons (xanthomas), and coronary arteries (atherosclerosis).
Test DetailsThe analysis includes the Factor V Leiden (R506Q), Protrombin (20210G>A), PAI (4G/5G) and MTHFR (677C>T).
Test DetailsThe analysis includes the base panel and ANXA5 (M1/M2 haplotype)
Test DetailsThe analysis is recommended in case of recurrent spontaneous abortions, preeclampsia and endometriosis - VEGFA (936C>T, VEGFA (-1154G>A), TAFI (+505A>G) и ANXA5 (M1-M2 Haplotype).
Test DetailsThe analysis includes the bace panel, ACE (I/D), Factor XIII (Val34Leu), MTHFR ( 1298A>C), and MTRR (66A>G) .
Test DetailsThe analysis includes the base panel, MTRR (66A>G) and MTHFR (1298A>C).
Test DetailsNeural tube defect; Vitamin exchange B12
Test DetailsDeficiency of antithrombin III is a major risk factor for venous thromboembolic disease. Two categories of AT-III deficiency have been defined on the basis of AT-III antigen levels in the plasma of affected individuals. The majority of AT-III deficiency families belong in the type I (classic) deficiency group and have a quantitatively abnormal phenotype in which antigen and heparin cofactor levels are both reduced to about 50% of normal. The second category of AT-III deficiency has been termed type II (functional) deficiency. Affected individuals from these kindreds produce dysfunctional AT-III molecules; they have reduced heparin cofactor activity levels (about 50% of normal) but levels of AT-III antigen are often normal or nearly normal.
Test Details