Add to ORKGFahr syndrome, a clinical entity that manifests with various signs and symptoms and has a familial predisposition is characterized by symmetric calcification of basal ganglia. It may present with neuropsychiatric, extrapyramidal and cerebellar symptoms. The etiology has not been defined yet. Three cases of Fahr syndrome; presenting with various clinical signs and psychiatric symptoms are reported in this article. The first case that occured following Brucella treatment and the other two occuring idiopathically are evaluated with a neuropsychiatric approach
Introduction. Fahr´s syndrome is a rare, slowly progressive, neurodegenerative disorder, characte...
Fahr’s disease is a rare syndrome characterized by symmetrical and bilateral intracranial calcificat...
Fahr syndrome is an idiopathic deposition of calcium in the basal ganglia (most commonly in the Glob...
Fahr syndrome, a clinical entity that manifests with various signs and symptoms and has a familial ...
Fahr syndrome which presents with various signs and symptoms has a familial predisposition and is ch...
Familial idiopathic basal ganglia calcification (FIBGC) or Fahr's syndrome is a rare disorder with v...
Fahr syndrome is a rare anatomo-clinical entity in pediatrics. Associating calcifications of the bas...
Fahr syndrome (FS) is a rare disorder where bilateral, almost symmetric, calcium and other mineral d...
Familial idiopathic basal ganglia calcification (Fahr's disease) is defined as basal ganglia, dentat...
Fahr syndrome is a rare condition mainly characterized by symmetric and bilateral calcification of b...
Fehr's disease, also known as Idiopathic Calcification of the Basal Ganglia (ICBG) or nonarterioscle...
Fahr’s disease is a rare idiopathic bilateral and symmetrical calcification of the basal gangli...
AbstractFahr's disease is a rare idiopathic degenerative neurological disorder, which can be present...
Fahr syndrome is a rare neurodegenerative disorder characterized by symmetrical, bilateral calcifica...
Fahr’s disease (FD) is characterized by sporadic or familiar idiopathic calcification of the basal g...
Introduction. Fahr´s syndrome is a rare, slowly progressive, neurodegenerative disorder, characte...
Fahr’s disease is a rare syndrome characterized by symmetrical and bilateral intracranial calcificat...
Fahr syndrome is an idiopathic deposition of calcium in the basal ganglia (most commonly in the Glob...
Fahr syndrome, a clinical entity that manifests with various signs and symptoms and has a familial ...
Fahr syndrome which presents with various signs and symptoms has a familial predisposition and is ch...
Familial idiopathic basal ganglia calcification (FIBGC) or Fahr's syndrome is a rare disorder with v...
Fahr syndrome is a rare anatomo-clinical entity in pediatrics. Associating calcifications of the bas...
Fahr syndrome (FS) is a rare disorder where bilateral, almost symmetric, calcium and other mineral d...
Familial idiopathic basal ganglia calcification (Fahr's disease) is defined as basal ganglia, dentat...
Fahr syndrome is a rare condition mainly characterized by symmetric and bilateral calcification of b...
Fehr's disease, also known as Idiopathic Calcification of the Basal Ganglia (ICBG) or nonarterioscle...
Fahr’s disease is a rare idiopathic bilateral and symmetrical calcification of the basal gangli...
AbstractFahr's disease is a rare idiopathic degenerative neurological disorder, which can be present...
Fahr syndrome is a rare neurodegenerative disorder characterized by symmetrical, bilateral calcifica...
Fahr’s disease (FD) is characterized by sporadic or familiar idiopathic calcification of the basal g...
Introduction. Fahr´s syndrome is a rare, slowly progressive, neurodegenerative disorder, characte...
Fahr’s disease is a rare syndrome characterized by symmetrical and bilateral intracranial calcificat...
Fahr syndrome is an idiopathic deposition of calcium in the basal ganglia (most commonly in the Glob...