Prevalence of Hemophilia A and B: Molecular and Clinical Similarities and Differences

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dc.contributor.authorHiba abu sharkh
dc.contributor.authorRuba Idrees
dc.contributor.authorShadia Al Najar
dc.contributor.authorKhawla Halahla
dc.contributor.authorLama Manasra
dc.contributor.authorYara Rawashdeh
dc.contributor.authorMayar Tarayrah
dc.contributor.authorAseel Shreteh
dc.contributor.authorHaneen Nur
dc.contributor.authorMahmoud Ramlawi
dc.date.accessioned2023-09-06T11:41:12Z
dc.date.available2023-09-06T11:41:12Z
dc.date.issued2023-05-16
dc.description.abstractBackground: Hemophilia A and B are rare congenital disorders linked to the X chromosome due to a lack or deficiency of clotting factor VIII (FVIII) or factor IX (FIX), respectively. The severity of the disease depends on decreased levels of factor VIII or factor IX, which are determined by the type of causative mutation in the gene coding factors (F8 and F9, respectively), and this can lead to spontaneous bleeding, as well as bleeding after injuries or surgery, given the importance of hemophilia. The old and recent studies aimed at identifying the disease and making society aware of it. Despite this, the Palestinian society lacks local awareness of this disease.
dc.description.sponsorshipAl-Quds University
dc.identifier.urihttps://dspace.alquds.edu/handle/20.500.12213/8621
dc.language.isoen
dc.publisherAl-Quds University - Deanship of Scientific Research
dc.titlePrevalence of Hemophilia A and B: Molecular and Clinical Similarities and Differences
dc.typeArticle
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