Fahr's disease (FD) or Fahr’s syndrome is characterized by basal ganglia calcification with clinical manifestations
in the form of neuropsychiatric disorders, neurological symptoms, and cognitive symptoms. FD commonly affects
young to middle aged adults. The etiology of this syndrome does not identify a specific agent. Clinical
manifestations of this disease incorporate a wide variety of symptoms. The diagnostic criteria of Fahr’s Syndrome
consist of bilateral calcification of basal ganglia, progressive neurologic dysfunction, absence of biochemical
abnormalities, infectious, traumatic, and a significant family history. Medical imaging techniques for the diagnosis
consist of computed tomography (CT), magnetic resonance imaging (MRI), and plain radiography of the skull. This
paper presents a case of Fahr’s syndrome in a 60-year-old married prisoner with antisocial personality and
seizures. Furthermore, CT and MRI scans showed bilateral symmetric calcifications in the basal ganglia
calcification (BGC) and dentate nuclei, cerebellum, and centrum semiovale
