Note: This case has been tagged as "legacy" as it no longer meets image preparation and/or other case publication guidelines.
From the case:
Fahr disease
{"current_user":null,"step_through_annotations":true,"access":{"can_edit":false,"can_download":true,"can_toggle_annotations":true,"can_feature":false,"can_examine_pipeline_reports":false,"can_pin":false},"extraPropsURL":"/studies/11010/annotated_viewer_json?_c=1689708900\u0026lang=us"}
Calcification in basal ganglia and cerebellum.
Case Discussion
Fahr disease (also known as familial cerebral ferrocalcinosis) is a congenital disorder characterized by abnormal calcium deposition with subsequent atrophy involving the basal ganglia +/- cerebral and cerebellar cortical regions.