Pyridoxine dependent seizures magnetic resonance spectroscopy findings

dc.authorid7768en_US
dc.contributor.authorAlkan, Alpay
dc.contributor.authorKutlu, Ramazan
dc.contributor.authorSığırcı, Ahmet
dc.contributor.authorOrkan, İsmet
dc.contributor.authorYakıncı, Mehmet Cengiz
dc.date.accessioned2017-06-23T11:46:33Z
dc.date.available2017-06-23T11:46:33Z
dc.date.issued2004
dc.departmentİnönü Üniversitesien_US
dc.description.abstractPyridoxine-dependent seizures are an extremely rare genetic disorder. Early diagnosis and treatment are important for the prevention of permanent brain damage. Elevated levels of glutamate and decreased levels of -aminobutyric acid (GABA) in the frontal and parietal cortices are among the characteristic features of this disorder. These metabolic abnormalities eventually lead to seizures and neuronal loss. In this case report, we present magnetic resonance spectroscopy findings of a 9-year-old girl with pyridoxine-dependent seizures with mental retardation. The N-acetylaspartate-to-creatine ratio was found to be decreased in the frontal and parieto-occipital cortices, which could indicate neuronal loss. Magnetic resonance spectroscopy could be a useful tool in the neuroimaging evaluation for assessment of parenchymal changes despite a normal-appearing brain magnetic resonance image in patients with pyridoxine-dependent seizures.en_US
dc.identifier.citationAlkan, A. Kutlu, R. Sığırcı, A. Orkan, İ. Yakıncı, M. C. (2004). Pyridoxine dependent seizures magnetic resonance spectroscopy findings. J Child Neurol. 19, (1).;75-78.en_US
dc.identifier.endpage78en_US
dc.identifier.issue1en_US
dc.identifier.startpage75en_US
dc.identifier.urihttps://hdl.handle.net/11616/7163
dc.identifier.volume19en_US
dc.language.isoenen_US
dc.publisherJ Child Neurolen_US
dc.relation.ispartofJ Child Neurolen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titlePyridoxine dependent seizures magnetic resonance spectroscopy findingsen_US
dc.typeArticleen_US

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