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dc.contributor.authorErdincler, P
dc.contributor.authorCiplak, N
dc.contributor.authorCanbaz, B
dc.contributor.authorKaynar, MY
dc.contributor.authorDashti, R
dc.contributor.authorKuday, C
dc.date.accessioned2021-03-03T15:05:33Z
dc.date.available2021-03-03T15:05:33Z
dc.date.issued1997
dc.identifier.citationErdincler P., Dashti R., Kaynar M., Canbaz B., Ciplak N., Kuday C., "Hydrocephalus and chronically increased intracranial pressure in achondroplasia", CHILDS NERVOUS SYSTEM, cilt.13, sa.6, ss.345-348, 1997
dc.identifier.issn0256-7040
dc.identifier.otherav_3d1e1eef-b043-48b8-a7b1-b4b413c29c83
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/44991
dc.identifier.urihttps://doi.org/10.1007/s003810050094
dc.description.abstractTwo achondroplastic children with ventriculomegaly are reported. The patients had no signs of increased intracranial pressure, but in one blindness had previously been detected by the parents. Neuroradiological examinations showed ventriculomegaly in both. Intracranial pressure remained at high levels (20-55 mmHg) preoperatively; ventriculo-peritoneal shunting was performed in both cases, and postoperatively levels fell to normal (5-16 mmHg). The need for the treatment of ventriculomegaly seen in achondroplastic children is analyzed on the basis of these two patients, with a brief review of literature.
dc.language.isoeng
dc.subjectCERRAHİ
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectNöroloji
dc.subjectCerrahi Tıp Bilimleri
dc.subjectPEDİATRİ
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectKLİNİK NEUROLOJİ
dc.titleHydrocephalus and chronically increased intracranial pressure in achondroplasia
dc.typeMakale
dc.relation.journalCHILDS NERVOUS SYSTEM
dc.contributor.department, ,
dc.identifier.volume13
dc.identifier.issue6
dc.identifier.startpage345
dc.identifier.endpage348
dc.contributor.firstauthorID118983


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