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- W1997952519 abstract "Alexander disease (fibrinoid leucodystrophy; originally described by Alexander in 1949) is a rare, fatal, nonfamilial leucoencephalopathy caused by astrocyte dysfunction characterised by missense mutation in the genes coding for glial fibrillary acidic protein(GFAP). It typically presents with frontal preponderance of white matter abnormalities and macroencephaly. We report a case of leucoencephalopathy with macroencephaly that shows characteristic MRI features of Alexander disease." @default.
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- W1997952519 date "2012-09-10" @default.
- W1997952519 modified "2023-09-25" @default.
- W1997952519 title "MRI diagnosis of Alexander disease" @default.
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- W1997952519 doi "https://doi.org/10.4102/sajr.v16i3.296" @default.
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