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.
- Definition Familial Idiopathic Basal Ganglia Calcification:
- Dictionary Familial Idiopathic Basal Ganglia Calcification - See Fahr's Syndrome above fahr's syndrome explain.
- Definition Fisher Syndrome:
- Dictionary rare, acquired nerve disease that is considered to be a variant of Guillain-Barre syndrome. It is characterized by abnormal muscle coordination, paralysis of the eye muscles, and absence of the fahr's syndrome what is.
- Definition Familial Hemangioma - Or Cavernous Malformation:
- Dictionary or Cavernous malformation, is a rare disorder of the capillaries and smallest veins in one part of the brain. The disorder occurs when a blood-filled mass resembling a tumor, called a hemangioma fahr's syndrome meaning.
