From Mild Ataxia to Huntington Disease Phenocopy: The Multiple Faces of Spinocerebellar Ataxia 17

Figure 1

(a) Pedigree of the Greek family with a SCA 17 expansion. (b) PCR products of the two affected sisters and a normal control run with markers on a 4% agarose gel. (c) Brain MRI of case III-4 (index case) showing significant cerebellar atrophy and mild brainstem and cerebral atrophy. (d) Brain MRI of case III-3 showing significant cerebellar atrophy and mild brainstem atrophy.

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