Trombofilia ereditară apare datorită prezenței unor anomalii genetice, care intervin în sinteza unor proteine cu rol în coagluare. Cele mai des întâlnite forme sunt: factorul V Leiden; mutaţiile genei protrombinei. Rareori pot fi întâlnite si。
indicatii: investigatie utila pentru stabilirea profilului genetic al riscului de trombofilie. Sunt inclusi urmatorii parametrii: mutatia T1565C / GPIIIa (glicoproteina IIIa) – glicoproteina (Gp) IIb/IIIa。
Profil trombofilie ereditara contine: Antitrombina III Proteina C Proteina S Mutatia factorului V Leiden – detectie si genotipare Mutatia protrombinica (factor II) Gena profil trombofilie ereditaraMTHFR (mutatii C677T; A1298C) – risc trombofilie
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