Hematology and coagulation

The test detects a gene mutation thatóra causes factor XIII clotting deficiency, a rare inherited blood clotting disorder in which factor XIII, a protein in the blood responsible for stabilizing the clot, malfunctions or is present in insufficient amounts.

The test allows to determine the ability of immune cellsórek to have an oxygen burst i.e. produce reactive oxygen species, which determines their ability to kill engulfed bacteria and overcome infection. The test is used in the diagnosis of immune disorders

Balk C antigen test measures the concentration of protein C, important for blood clotting. The test is done to clarify the cause of a thromboembolic incident to see if there is an inherited or acquired deficiencyór of protein C.

A blood test that measures the level of a substance called factor IX inhibitor, whichóra is important for blood clotting.

Testing in the blood of a substance called human clotting factor XIII, which is involved in the blood clotting process, responsible for stabilizing the clot.

The blood test is performed to diagnose clotting deficienciesós, it measures the level of alpha 2-antiplasmin, a protein thatóre inhibits fibrinolysis i.e. the dissolution of a blood clot, a deficiencyór of this protein can cause bleeding or hemorrhages into jointsós.

The test detects LE cellsórek - these are white blood cells that have engulfed and processed cellsór of another specific type. The test is used to diagnose an autoimmune disease - systemic lupus erythematosus (SLE).

The test is part of a complete blood count, ordered as part of a routine checkup, and assesses the number of special cellsórecords in the blood, called platelets or thrombocytes, to evaluate the function of the clotting system.

The test involves determining the blood level of an enzyme called glucose-6-phosphate dehydrogenase, important for red blood cell metabolism, in order to diagnose a deficiency of this enzyme, which causes neonatal jaundiceó and other disorders