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Acquired Chiari I Malformation Secondary to Spontaneous Intracranial Hypotension Syndrome and Persistent Hypoglycemia: A Case Report

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dc.contributor.authorOnal, Hasan
dc.contributor.authorErsen, Atilla
dc.contributor.authorGemici, Hakan
dc.contributor.authorAdal, Erdal
dc.contributor.authorGuler, Serhat
dc.contributor.authorSander, Serdar
dc.contributor.authorAlbayram, Sait
dc.date.accessioned2020-10-22T15:56:02Z
dc.date.available2020-10-22T15:56:02Z
dc.date.issued2018-12-01T00:00:00Z
dc.description.abstractSpontaneous intracranial hypotension (SIH) is a rare and potentially serious condition in childhood. Cerebrospinal fluid (CSF) volume depletion is thought to be the main causative feature for intracranial hypotension and results from a spontaneous CSF leak, often at the spine level. SIH is increasingly diagnosed in clinical practice, although it manifests a varied symptomatology. The downward displacement of the brain, sometimes mimicking a Chiari I malformation, has rarely been reported. We present a case of a SIH with Chiari I malformation accompanied by an unusual clinical presentation of persistent hypoglycemia.
dc.identifier.citationOnal H., Ersen A., Gemici H., Adal E., Guler S., Sander S., Albayram S., -Acquired Chiari I Malformation Secondary to Spontaneous Intracranial Hypotension Syndrome and Persistent Hypoglycemia: A Case Report-, JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, cilt.10, ss.391-394, 2018
dc.identifier.doi10.4274/jcrpe.0042
dc.identifier.pubmed29513222
dc.identifier.scopus85057565929
dc.identifier.trdizinDOI: https://doi.org/10.4274/jcrpe.0042
dc.identifier.urihttp://hdl.handle.net/20.500.12645/23679
dc.identifier.wosWOS:000451667000015
dc.rightsinfo:eu-repo/semantics/openAccess
dc.titleAcquired Chiari I Malformation Secondary to Spontaneous Intracranial Hypotension Syndrome and Persistent Hypoglycemia: A Case Report
dc.typeArticle
dspace.entity.typePublication
local.avesis.id4ea20226-16f6-48b5-9ba8-a17ca7f34087
local.publication.isinternational1
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