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Cerebellar vermian hypoplasia in a Cocker Spaniel

DC Field Value Language
dc.contributor.authorLim, Ji-Hey-
dc.contributor.authorKim, Dae-Yong-
dc.contributor.authorYoon, Junghee-
dc.contributor.authorKim, Wan Hee-
dc.contributor.authorKweon, Oh Kyeong-
dc.date.accessioned2009-08-25T07:38:26Z-
dc.date.available2009-08-25T07:38:26Z-
dc.date.issued2008-
dc.identifier.citationJ. Vet. Sci. 2008, 9, 215-217en
dc.identifier.issn1229-845X-
dc.identifier.urihttp://www.vetsci.org/2008/abstract/215a.html-
dc.identifier.urihttp://hdl.handle.net/10371/7780-
dc.description.abstractAn eight-week-old female Cocker Spaniel was presented with ataxia, dysmetria and intention tremor. At 16 weeks, the clinical signs did not progress. Investigation including imaging studies of the skull and cerebrospinal fluid analysis were performed. The computed tomography revealed a cyst-like dilation at the level of the fourth ventricle associated with vermal defect in the cerebellum. After euthanasia, a cerebellar hypoplasia with vermal defect was identified on necropsy. A polymerase chain reaction amplification of cerebellar tissue revealed the absence of an in utero parvoviral infection. Therefore, the cerebellar hypoplasia in this puppy was consistent with diagnosis of primary cerebellar malformation comparable to Dandy-Walker syndrome in humans..en
dc.language.isoen-
dc.publisher대한수의학회 = The Korean Society of Veterinary Scienceen
dc.subjectcerebellar hypoplasiaen
dc.subjectdogen
dc.subjectvermian defecten
dc.titleCerebellar vermian hypoplasia in a Cocker Spanielen
dc.typeArticleen
dc.contributor.AlternativeAuthor임지혜-
dc.contributor.AlternativeAuthor김대용-
dc.contributor.AlternativeAuthor윤정희-
dc.contributor.AlternativeAuthor김완희-
dc.contributor.AlternativeAuthor권오경-
Appears in Collections:
College of Veterinary Medicine (수의과대학)Dept. of Veterinary Medicine (수의학과)Journal Papers (저널논문_수의학과)
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