Infantile sandhoff s disease multivoxel magnetic resonance spectroscopy findings
Yükleniyor...
Dosyalar
Tarih
2003
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
J Child Neurol
Erişim Hakkı
info:eu-repo/semantics/openAccess
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
Kaynak
J Child Neurol
WoS Q Değeri
Scopus Q Değeri
Cilt
18
Sayı
Künye
Alkan, A. Kutlu, R. Yakıncı, M. C. Sığırcı, A. Aslan, M. Saraç, K. (2003). Infantile sandhoff s disease multivoxel magnetic resonance spectroscopy findings. J Child Neurol. 18:425–428.
