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 …

Purpose of review There is growing interest in disorders involved in ectopic mineralization.
Fahr disease or idiopathic basal ganglia calcification can serve as a model for ectopic …

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

Mutations in XPR1, a gene encoding an inorganic phosphate exporter, have recently been
identified in patients with primary familial brain calcification (PFBC). Using Sanger …

Objective: To investigate the clinical, genetic, and neuroradiologic presentations of
idiopathic basal ganglia calcification (IBGC) in a nationwide study in Japan. Methods: We …

Familial idiopathic basal ganglia calcification (FIBGC), also known as “Fahr's disease,” is a
neuropsychiatric disorder with motor and cognitive symptoms. It is characterized …

Objective: Fahr disease (FD) is a rare neurological and psychiatric disorder. The disease is
classified by intracranial calcification of the basal ganglia with the globus pallidus region …

Calcification of basal ganglia or Fahr's syndrome is a rare disease characterized by bilateral
and symmetrical intracranial deposition of calcium mainly in cerebral basal ganglia. Motor …

Idiopathic basal ganglia calcification (IBGC) is a rare neurodegenerative disorder
characterized by the deposition of calcium in the brain and variable combinations of …

Idiopathic basal ganglia calcification or Fahr's disease is a neurological condition with a
prominent movement disorder. Diagnostically, brain imaging with computerized tomographic …