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dc.contributor.editorPant, Sadip
dc.contributor.editorCherian, Iype
dc.date.accessioned2021-04-20T15:21:38Z
dc.date.available2021-04-20T15:21:38Z
dc.date.issued2012
dc.identifierONIX_20210420_9789535101628_977
dc.identifier.urihttps://directory.doabooks.org/handle/20.500.12854/65620
dc.description.abstractDescription of hydrocephalus can be found in ancient medical literature from Egypt as old as 500 AD. Hydrocephalus is characterized by abnormal accumulation of cerebrospinal fluid (CSF) in the ventricles of the brain. This results in the rise of intracranial pressure inside the skull causing progressive increase in the size of the head, seizure, tunneling of vision, and mental disability. The clinical presentation of hydrocephalus varies with age of onset and chronicity of the underlying disease process. Acute dilatation of the ventricular system manifests with features of raised intracranial pressure while chronic dilatation has a more insidious onset presenting as Adams triad. Treatment is generally surgical by creating various types of cerebral shunts. Role of endoscopic has emerged lately in the management of hydrocephalus.
dc.languageEnglish
dc.subject.classificationthema EDItEUR::M Medicine and Nursing::MJ Clinical and internal medicine::MJG Endocrinologyen_US
dc.subject.otherEndocrinology
dc.titleHydrocephalus
dc.typebook
oapen.identifier.doi10.5772/1212
oapen.relation.isPublishedBy78a36484-2c0c-47cb-ad67-2b9f5cd4a8f6
oapen.relation.isbn9789535101628
oapen.relation.isbn9789535152125
oapen.imprintIntechOpen
oapen.pages228


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