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| Fahr disease ： ウィキペディア英語版 |
Fahr's syndrome
Idiopathic Basal Ganglia Calcification, also known as Fahr disease, is a rare,〔http://rarediseases.info.nih.gov/GARD/Disease.aspx?PageID=4&diseaseID=8272〕 genetically dominant, inherited neurological disorder characterized by abnormal deposits of calcium in areas of the brain that control movement. Through the use of CT scans, calcifications are seen primarily in the basal ganglia and in other areas such as the cerebral cortex.
==Symptoms==
Symptoms of this disease include deterioration of motor functions and speech, seizures, and other involuntary movement. Other symptoms are headaches, dementia, and vision impairment.
Characteristics of Parkinson's Disease are also similar to Fahr's Syndrome. 〔(【引用サイトリンク】url=http://www.ninds.nih.gov/disorders/fahrs/fahrs.htm )〕
抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』
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