Fig. 1From: A novel mutation in RNF216 gene in a Turkish case with Gordon Holmes syndromeMRI of the case in 2018 and 2022. According to 2018 (a, axial T2 and b, sagittal T1-weighted) MRI in 2022 (c axial, d sagittal T2-weighted) progression is seen in cerebellar, vermian and cerebral cortical atrophy. Mild atrophy in the mesencephalon has not progressedBack to article page