Fahr syndrome which presents with various signs and symptoms has a familial predisposition and is characterized by symmetric calcification of basal ganglia. It may present with neuropsychiatric, extrapyramidal, and cerebellar symptoms. The etiology has not been defined yet. A 38-year-old woman referred to the psychiatric clinic of 5th Azar Hospital, Gorgan, Iran, with neuropsychiatric presentation
Fahr’s disease is a rare syndrome characterized by symmetrical and bilateral intracranial calcificat...
Fahr's syndrome is a fairly rare antomo-clinic entity, it is defined by the existence of bilateral a...
Fahr’s disease (FD) is characterized by sporadic or familiar idiopathic calcification of the basal g...
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, a clinical entity that manifests with various signs and symptoms and has a familial ...
Fahr syndrome is a rare anatomo-clinical entity in pediatrics. Associating calcifications of the bas...
Fahr’s disease is rare degenerative, neurological disorder characterized by idiopathic intra-cranial...
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...
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...
Fahr syndrome is a rare condition mainly characterized by symmetric and bilateral calcification of b...
Fahr’s syndrome is a rare neurodegenerative disorder characterized by bilateral basal ganglia calcif...
Fahr's disease or idiopathic basal ganglia calcification is a rare pathology. The most common clinic...
Fahr’s disease is a rare syndrome characterized by symmetrical and bilateral intracranial calcificat...
Fahr's syndrome is a fairly rare antomo-clinic entity, it is defined by the existence of bilateral a...
Fahr’s disease (FD) is characterized by sporadic or familiar idiopathic calcification of the basal g...
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, a clinical entity that manifests with various signs and symptoms and has a familial ...
Fahr syndrome is a rare anatomo-clinical entity in pediatrics. Associating calcifications of the bas...
Fahr’s disease is rare degenerative, neurological disorder characterized by idiopathic intra-cranial...
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...
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...
Fahr syndrome is a rare condition mainly characterized by symmetric and bilateral calcification of b...
Fahr’s syndrome is a rare neurodegenerative disorder characterized by bilateral basal ganglia calcif...
Fahr's disease or idiopathic basal ganglia calcification is a rare pathology. The most common clinic...
Fahr’s disease is a rare syndrome characterized by symmetrical and bilateral intracranial calcificat...
Fahr's syndrome is a fairly rare antomo-clinic entity, it is defined by the existence of bilateral a...
Fahr’s disease (FD) is characterized by sporadic or familiar idiopathic calcification of the basal g...