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Canavan Disease (Spongy Cerebral Degeneration) - A Case Report -

DC Field Value Language
dc.contributor.authorOh, Mee Hye-
dc.contributor.authorKim, Chong Jai-
dc.contributor.authorChi, Je G.-
dc.contributor.authorKim, In-One-
dc.contributor.authorHwang, Yong Seung-
dc.contributor.authorWang, Kyu Chang-
dc.contributor.authorCho, Byung Kyu-
dc.date.accessioned2009-08-10T07:10:56Z-
dc.date.available2009-08-10T07:10:56Z-
dc.date.issued1995-06-
dc.identifier.citationSeoul J Med, Vol.36 No.2, pp. 85-91-
dc.identifier.issn0582-6802-
dc.identifier.urihttps://hdl.handle.net/10371/6810-
dc.description.abstractWe report a case of Canavan disease in a 6 month-old male Korean
baby who presented with aggravating tonic-clonic seizure for 5 days. Pathologic'
findings could be summarized as follows; increase in brain volume and weight,
spongy degeneration in the deep layers of the cerebral cortex and subcortical
white matter, and hyperplasia of Alzheimer type II astrocytes throughout the cerebral
cortex. Ultrastructurally, there was an abnormal accumulation of fluid in
astrocytes and between splitting myelin lamellae.
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dc.language.isoen-
dc.publisherSeoul National University College of Medicine-
dc.subjectCanavan disease-
dc.subjectSpongy cerebral degeneration-
dc.subjectN-acetylaspartic acid-
dc.subjectAspartoacylase-
dc.titleCanavan Disease (Spongy Cerebral Degeneration) - A Case Report --
dc.typeSNU Journal-
dc.contributor.AlternativeAuthor오미혜-
dc.contributor.AlternativeAuthor김종재-
dc.contributor.AlternativeAuthor지제근-
dc.contributor.AlternativeAuthor김인원-
dc.contributor.AlternativeAuthor황용승-
dc.contributor.AlternativeAuthor왕규창-
dc.contributor.AlternativeAuthor조병규-
dc.citation.journaltitle서울 의대 잡지-
dc.citation.journaltitle서울 의대 학술지-
dc.citation.journaltitleSeoul Journal of Medicine-
dc.citation.endpage91-
dc.citation.number2-
dc.citation.pages85-91-
dc.citation.startpage85-
dc.citation.volume36-
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