What FAHR'S SYNDROME means: Fahr's Syndrome - also known as Idiopathic Basal Ganglia Calcification or Fahr's Syndrome is a rare, genetically dominant, inherited neurological disorder characterized by abnormal deposits of calcium in areas of the brain that control movement, including the basal ganglia and the cerebral cortex. Symptoms of the disorder may include deterioration of motor function, pychosis dementia, seizures, headache, dysarthria (poorly articulated speech), spasticity (stiffness of the limbs) and spastic paralysis, eye impairments, and athetosis (involuntary, writhing movements).
- Definition Farber'S Disease - Also Known As Farber'S Lipogranulomatosis Or Ceramidase Deficiency:
- Dictionary Disease - also known as Farber's lipogranulomatosis or ceramidase deficiency, describes a group of rare autosomal recessive disorders that cause an accumulation of lipids in the joints, tissues fahr's syndrome.
- Definition Febrile Seizures:
- Dictionary a convulsion in young children caused by a sudden spike in body temperature, often from an infection. During a febrile seizure, a child often loses consciousness and shakes, moving limbs on both fahr's syndrome.
- Definition Familial Periodic Paralyzes:
- Dictionary Paralyzes - are a group of inherited neurological disorders caused by mutations in genes that regulate sodium and calcium channels in nerve cells. They are characterized by episodes in which the fahr's syndrome.
- Definition Frontotemporal Dementia - (Frontotemporal Lobar Degeneration):
- Dictionary Dementia - (frontotemporal lobar degeneration) is an umbrella term for a diverse group of rare disorders that primarily affect the frontal and temporal lobes of the brain - the areas generally fahr's syndrome.