Adrenoleukodystrophy: single voxel MR spectroscopy findings (case report)
dc.authorscopusid | 7006266098 | |
dc.authorscopusid | 7003405757 | |
dc.authorscopusid | 57197007210 | |
dc.authorscopusid | 55928547600 | |
dc.contributor.author | Alkan A. | |
dc.contributor.author | Kutlu R. | |
dc.contributor.author | Aslan M. | |
dc.contributor.author | Yakinci C. | |
dc.date.accessioned | 2024-08-04T20:01:01Z | |
dc.date.available | 2024-08-04T20:01:01Z | |
dc.date.issued | 2004 | |
dc.department | İnönü Üniversitesi | en_US |
dc.description.abstract | Adrenoleukodystrophy is a rare genetic disorder. Histopathological features of this disorder include demyelination and axonal loss in white matter. We describe a six-year-old boy with significantly decreased N-acetyl-aspartate (NAA)/Creatin (Cr), increased Choline (Cho)/Cr and Myo-inositol (MI)/Cr in parieto-occipital white matter by MR spectroscopy. In contrast to the normal appearance of frontal white matter on MR imaging, increased Cho/Cr and MI/Cr ratios were detected on MR spectroscopy. These changes in involved areas could be an indication of neuroaxonal loss, demyelination and gliosis. | en_US |
dc.identifier.endpage | 203 | en_US |
dc.identifier.issn | 1300-4360 | |
dc.identifier.issue | 3 | en_US |
dc.identifier.pmid | 15470621 | en_US |
dc.identifier.scopus | 2-s2.0-7444229980 | en_US |
dc.identifier.scopusquality | N/A | en_US |
dc.identifier.startpage | 200 | en_US |
dc.identifier.uri | https://hdl.handle.net/11616/91201 | |
dc.identifier.volume | 10 | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.language.iso | tr | en_US |
dc.relation.ispartof | Tanisal ve girişimsel radyoloji : Tibbi Görüntüleme ve Girişimsel Radyoloji Dernegi yayin organi | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | adrenoleukodystrophy | en_US |
dc.subject | article | en_US |
dc.subject | case report | en_US |
dc.subject | child | en_US |
dc.subject | differential diagnosis | en_US |
dc.subject | human | en_US |
dc.subject | male | en_US |
dc.subject | nuclear magnetic resonance imaging | en_US |
dc.subject | pathology | en_US |
dc.subject | Adrenoleukodystrophy | en_US |
dc.subject | Child | en_US |
dc.subject | Diagnosis, Differential | en_US |
dc.subject | Humans | en_US |
dc.subject | Magnetic Resonance Imaging | en_US |
dc.subject | Male | en_US |
dc.title | Adrenoleukodystrophy: single voxel MR spectroscopy findings (case report) | en_US |
dc.title.alternative | Adrenolökodistrofi: tek voksel MR spektroskopi bulgulari. | en_US |
dc.type | Article | en_US |