Fahr disease

Case contributed by Dr Hani Salam
Modality: CT

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.

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Case Information

rID: 36463
Case created: 24th Apr 2015
Last edited: 11th Sep 2015
Inclusion in quiz mode: Included

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