Fig. 1From: A case of dystonia with polycythemia and hypermanganesemia caused by SLC30A10 mutation: a treatable inborn error of manganese metabolismBrain MRI of the patient showed symmetric hyperintensities of the basal ganglia, tectum of the pons, and dentate nucleuses on T1- W images (a) and a normal appearance on T2-W images (b). Repeated brain MRI at 6 months follow-up showed significant resolution of previous findings on T1 images (c)Back to article page