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Fig. 2 | Human Genomics

Fig. 2

From: The genetic basis of early-onset hereditary ataxia in Iran: results of a national registry of a heterogeneous population

Fig. 2

MRI of patients with c.574T > C (CWF19L1) variant (a-c), c.388G > A (THG1L) variant (d,e), c.1781G > A (DARS2) variant (f, g) and c.398 A > G (BRAT1); (a) Axial T2-Weighted Brain MRI shows increased peri-vascular spaces. (b) Sagittal and (c) Coronal T2- Weighted Imaging shows cerebellar (prominently vermis) atrophy. d and e) T2-weighted sagittal and coronal images showing cerebellar atrophy. f) Coronal T2-Weighted Brain MRI is indicative of white matter, internal capsule and bilateral dentate involvement. g) Sagittal T2-Weighted view shows corpus callosum atrophy. h) Sagittal and i) Coronal T2-Weighted Brain MRI shows severe cerebellar atrophy

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Human Genomics

ISSN: 1479-7364