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dc.contributor.authorDikici, Suleyman
dc.contributor.authorOzer, Harun
dc.contributor.authorGulertan, Serap Yavuz
dc.contributor.authorYuksel, Adnan
dc.contributor.authorBas, Ahmet
dc.contributor.authorAlbayram, Sait
dc.date.accessioned2021-03-03T18:24:11Z
dc.date.available2021-03-03T18:24:11Z
dc.date.issued2008
dc.identifier.citationAlbayram S., Bas A., Ozer H., Dikici S., Gulertan S. Y. , Yuksel A., "Spontaneous intracranial hypotension syndrome in a patient with Marfan syndrome and autosomal dominant polycystic kidney disease", HEADACHE, cilt.48, sa.4, ss.632-636, 2008
dc.identifier.issn0017-8748
dc.identifier.otherav_4ece9282-0a5c-4be3-8606-69a8231be5e2
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/56269
dc.identifier.urihttps://doi.org/10.1111/j.1526-4610.2007.01033.x
dc.description.abstractIntracranial hypotension is typically manifested by orthostatic headache. The most frequent underlying factor is cerebrospinal fluid leakage. It has been suggested that dural structural weakness in some connective tissue diseases may be responsible for dural tears and diverticula and consequently leakage. We present a case of spontaneous intracranial hypotension associated with Marfan syndrome and autosomal dominant polycystic kidney disease. The patient was treated successfully with epidural autologous blood patch. Dural involvements of these hereditary connective tissue diseases are also discussed.
dc.language.isoeng
dc.subjectNöroloji
dc.subjectDahili Tıp Bilimleri
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectKLİNİK NEUROLOJİ
dc.titleSpontaneous intracranial hypotension syndrome in a patient with Marfan syndrome and autosomal dominant polycystic kidney disease
dc.typeMakale
dc.relation.journalHEADACHE
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume48
dc.identifier.issue4
dc.identifier.startpage632
dc.identifier.endpage636
dc.contributor.firstauthorID187217


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