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dc.contributor.authorUysal, Serap
dc.contributor.authorErcan, Tugba Erener
dc.contributor.authorAlbayram, Sait
dc.date.accessioned2021-03-03T14:48:07Z
dc.date.available2021-03-03T14:48:07Z
dc.date.issued2008
dc.identifier.citationUysal S., Albayram S., Ercan T. E. , "Spontaneous Intracranial Hypotension: A Case Report", JOURNAL OF CHILD NEUROLOGY, cilt.23, sa.11, ss.1312-1315, 2008
dc.identifier.issn0883-0738
dc.identifier.otherav_3b80b983-637f-4326-ab96-58fc2381cb26
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/43957
dc.identifier.urihttps://doi.org/10.1177/0883073808318051
dc.description.abstractSpontaneous intracranial hypotension is a rare syndrome of low ccrebrospinal fluid pressure due to spontaneous cerebrospinal fluid leaks. The main feature is orthostatic headache. We describe a case of spontaneous intracranial hypotension in a 5-year-old girl with a 1-month history of headache, sudden onset hearing loss, and ataxia. Magnetic resonance imaging (MRI) showed an enlargement of cervical venous plexus and lumbar puncture revealed a low opening pressure. Magnetic resonance myelography showed leakage of the contrast material at the level of the third and fourth lumbar vertebra. Bed rest and caffeine treatment yielded no resolution of symptoms. Following a lumbar epidural blood patch, her headache and ataxia resolved completely without any improvement in hearing. A second blood patch also yielded no effect on hearing. Spontaneous intracranial hypotension should be considered in the differential diagnosis of headache, also in the pediatric age group.
dc.language.isoeng
dc.subjectNöroloji
dc.subjectTıp
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectPEDİATRİ
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectKLİNİK NEUROLOJİ
dc.titleSpontaneous Intracranial Hypotension: A Case Report
dc.typeMakale
dc.relation.journalJOURNAL OF CHILD NEUROLOGY
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume23
dc.identifier.issue11
dc.identifier.startpage1312
dc.identifier.endpage1315
dc.contributor.firstauthorID190048


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