Infantile Sandhoff's disease: Multivoxel magnetic resonance spectroscopy findings
Küçük Resim Yok
Tarih
2003
Yazarlar
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
B C Decker Inc
Erişim Hakkı
info:eu-repo/semantics/closedAccess
Özet
Sandhoff's disease is a rare, genetic lysosomal storage disease leading to delayed myelination or demyelination. Although neuroimaging findings in this disease have been reported previously, magnetic resonance spectroscopy findings have not been reported. In this report, we present magnetic resonance imaging and magnetic resonance spectroscopy features of two cases with Sandhoff's disease. Magnetic resonance spectroscopy revealed findings indicating widespread demyelination in both cases and neuroaxonal loss and anaerobic metabolism in the second case. Magnetic resonance spectroscopy could provide useful information in the explanation of the clinical picture of cases with Sandhoff's disease.
Açıklama
Anahtar Kelimeler
[No Keywords]
Kaynak
Journal of Child Neurology
WoS Q Değeri
Q3
Scopus Q Değeri
N/A
Cilt
18
Sayı
6
