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. 2019 May 2;19(3):196–207. doi: 10.1136/practneurol-2018-002096

Table 2.

Diagnostic clues from MR scanning of the brain

Condition MR brain scan finding(s) MRI sequence
‘Diagnostic’
Multiple systems atrophy type C ‘Hot-cross bun’ sign*; pontine atrophy (figure 1) T2/FLAIR
Fragile X tremor-ataxia syndrome Middle cerebellar peduncle sign† (figure 2) T2/FLAIR
Superficial siderosis Deposition of haemosiderin; cerebellar atrophy (figure 3) GRE/T2*
Sporadic Creutzfeldt-Jakob disease High basal ganglia signal; cortical high (and persistent DWI) signal T2/FLAIR, DWI/ADC
Autosomal recessive spastic ataxia of Charlevoix-Saguenay Hypointense pontine stripes (figure 4); atrophy of superior cerebellar vermis; thinning of posterior mid-body of corpus callosum T2/FLAIR
SPG7 High dentate nuclei signal (figure 5)38 T2/FLAIR
‘Suggestive’ (in familial forms)
Friedreich’s ataxia, vitamin E deficiency Upper cervical cord atrophy; cerebellar atrophy late (figure 6) T1/T2
Ataxia-telangiectasia, ataxia with oculomotor apraxia, types 1 and 2 Cerebellar atrophy T1/T2
Autosomal dominant spinocerebellar ataxia Cerebellar and pontine atrophy T1/T2

*Also occurs in autosomal dominant spinocerebellar ataxia.

†Can occur in multiple systems atrophy type C.

ADC, apparent diffusion coefficient; DWI, diffusion-weighted imaging; FLAIR, fluid-attenuated inversion recovery; GRE, gradient echo; SPG7, spastic paraplegia 7.