Giant axonal neuropathy diffusion weighted imaging features of the brain

dc.authorid7768en_US
dc.contributor.authorAlkan, Alpay
dc.contributor.authorSığırcı, Ahmet
dc.contributor.authorKutlu, Ramazan
dc.contributor.authorDoğanay, Selim
dc.contributor.authorErdem, Gülnur
dc.contributor.authorYakıncı, Mehmet Cengiz
dc.date.accessioned2017-06-23T07:48:32Z
dc.date.available2017-06-23T07:48:32Z
dc.date.issued2006
dc.departmentİnönü Üniversitesien_US
dc.description.abstractGiant axonal neuropathy is a rare autosomal recessive childhood disorder characterized by a peripheral neuropathy and features of central nervous system involvement. Magnetic resonance imaging (MRI) of an 11-year-old boy with giant axonal neuropathy revealed high signal intensity in the white matter of the cerebrum and cerebellum on T2-weighted imaging. An apparent diffusion coefficient map revealed increased apparent diffusion coefficient values in the periventricular, deep, and cerebellar white matter, basal ganglia, and thalamus. Increased apparent diffusion coefficient values in distinct locations suggest increased mobility of water molecules in the brain of a patient with giant axonal neuropathy. This finding could indicate a myelin disorder such as demyelination. Diffusion-weighted imaging should be performed to reveal apparent diffusion coefficient changes and determine brain involvement in patients with giant axonal neuropathy.en_US
dc.identifier.citationAlkan, A. Sığırcı, A. Kutlu, R. Doğanay, S. Erdem, G. Yakıncı, M. C. (2006). Giant axonal neuropathy diffusion weighted imaging features of the brain. J Child Neurol. 21; 912–915.en_US
dc.identifier.doi10.2310/7010.2006.00211en_US
dc.identifier.endpage915en_US
dc.identifier.startpage912en_US
dc.identifier.urihttps://hdl.handle.net/11616/7151
dc.identifier.volume21en_US
dc.language.isoenen_US
dc.publisherJ Child Neurolen_US
dc.relation.ispartofJ Child Neurolen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleGiant axonal neuropathy diffusion weighted imaging features of the brainen_US
dc.typeArticleen_US

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