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 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.
- Definition Friedreich'S Ataxia:
- Dictionary Ataxia - an inherited disease that causes progressive damage to the nervous system resulting in symptoms ranging from gait disturbance and speech problems to heart disease. Symptoms usually begin fahr's syndrome explain.
- Definition Fabry Disease:
- Dictionary caused by the lack of or faulty enzyme needed to metabolize lipids, fat-like substances that include oils, waxes, and fatty acids. The enzyme is known as ceramide trihexosidase, also called alpha fahr's syndrome what is.
- 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 meaning.
