Basal ganglia calcifications could be incidental findings up to 20% of asymptomatic patients
undergoing CT or MRI scan. The presence of neuropsychiatric symptoms associated with …

Familial idiopathic basal ganglia calcification (Fahr's disease) is a rare neurodegenerative
disorder characterized by symmetrical and bilateral calcification of the basal ganglia …

Introduction There are now a number genes, known to be associated with familial primary
brain calcification (PFBC), causing the so called 'Fahr's' disease or syndrome. These are …

Idiopathic basal ganglia calcification is characterized by mineral deposits in the brain, an
autosomal dominant pattern of inheritance in most cases and genetic heterogeneity. The first …

Abstract Twenty-two patients aged 36–63 years were diagnosed as having Fahr's syndrome
on the basis of the presence on CT of unexpected extensive calcification of the basal …

Fahr's disease or Fahr's syndrome is a rare, neurological disorder characterized by
abnormal calcified deposits in basal ganglia and cerebral cortex. Calcified deposits are …

Familial idiopathic basal ganglia calcification (IBGC) or Fahr's disease is a rare
neurodegenerative disorder characterized by calcium deposits in the basal ganglia and …

Primary familial brain calcification (PFBC), also known as Fahr's disease, is a rare inherited
disorder characterized by bilateral calcification in the basal ganglia according to …

Of 7040 patients who were examined with CT scan for various reasons, 72 (1.02%) showed
symmetrical intracranial calcifications. On the basis of the extent of the calcifications, the …

Idiopathic basal ganglia calcification (IBGC) is characterised by radiological, neurological,
cognitive and psychiatric abnormalities. The associations between these abnormal …