Observation of Thrombophilia Testing Panel among Hebron Population

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dc.contributor.authorRaghad Al-Shareef
dc.contributor.authorDania Ewadeh
dc.contributor.authorMariam Shehada
dc.contributor.authorAhmad Salhab
dc.contributor.authorMohamad Sleimeih
dc.contributor.authorAshraf Abdeen
dc.contributor.authorRozan Attili
dc.date.accessioned2023-09-06T11:46:48Z
dc.date.available2023-09-06T11:46:48Z
dc.date.issued2023-05-16
dc.description.abstractBackground: Thrombophilia is abnormal blood coagulation that leads to an increased risk of blood tendency to clot. Genetic factors tested as a whole panel consist of seven genetic abnormalities: Factor V Leiden, Factor V, Prothrombin (Factor II), Beta Fibrinogen, Factor 8, MTHFR (C677T), MTHFR (A1298C), and four risk factors: Human Platelet Antigen, Angiotensin-converting enzyme (ACE), Glycoprotein IIIa (GP IIIa) and Plasminogen Activator Inhibitor-1 (PAI-1). In some cases protein c, protein s and Antithrombin may be added.
dc.description.sponsorshipAl-Quds University
dc.identifier.urihttps://dspace.alquds.edu/handle/20.500.12213/8623
dc.language.isoen
dc.publisherAl-Quds University - Deanship of Scientific Research
dc.titleObservation of Thrombophilia Testing Panel among Hebron Population
dc.typeArticle
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