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. 2022 Jan;43(1):2–10. doi: 10.3174/ajnr.A7362

FIG 4.

FIG 4.

A 1-year-old girl with a RNASEH2B mutation. There are patchy WMH throughout the brain. Symmetric T2-signal abnormality is noted in the globus pallidus, thalamus, and dentate nucleus. There is global cerebral volume loss. CT confirms basal ganglia calcifications.