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Plasminogen deficiency

dc.contributor.authorCelkan, Tiraje
dc.date.accessioned2021-03-03T07:42:30Z
dc.date.available2021-03-03T07:42:30Z
dc.date.issued2017
dc.identifier.citationCelkan T., "Plasminogen deficiency", JOURNAL OF THROMBOSIS AND THROMBOLYSIS, cilt.43, sa.1, ss.132-138, 2017
dc.identifier.issn0929-5305
dc.identifier.otherav_13653eed-cecd-4108-9a09-5539b560a4b5
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/18500
dc.identifier.urihttps://doi.org/10.1007/s11239-016-1416-6
dc.description.abstractPlasminogen plays an important role in fibrinolysis as well as wound healing, cell migration, tissue modeling and angiogenesis. Congenital plasminogen deficiency is a rare autosomal recessive disorder that leads to the development of thick, wood-like pseudomembranes on mucosal surfaces, mostly seen in conjunctivas named as "ligneous conjunctivitis". Local conjunctival use of fresh frozen plazma (FFP) in combination with other eye medications such as cyclosporin and artificial tear drops may relieve the symptoms. Topical treatment with plasminogen eye drops is the most promising treatment that is not yet available in Turkey.
dc.language.isoeng
dc.subjectDahili Tıp Bilimleri
dc.subjectCARDIAC ve CARDIOVASCULAR SİSTEMLER
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectHEMATOLOJİ
dc.subjectTıp
dc.subjectKardiyoloji
dc.subjectHematoloji
dc.subjectSağlık Bilimleri
dc.subjectİç Hastalıkları
dc.subjectPERİFERAL VASKÜLER HASTALIĞI
dc.titlePlasminogen deficiency
dc.typeMakale
dc.relation.journalJOURNAL OF THROMBOSIS AND THROMBOLYSIS
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume43
dc.identifier.issue1
dc.identifier.startpage132
dc.identifier.endpage138
dc.contributor.firstauthorID238465


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