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Medical Dictionary

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Fahr syndrome

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Fahr syndrome A rare, inherited, progressive brain disorder that is characterized clinically by involuntary movements, prolonged muscle contractions, and dementia. It is characterized by abnormal deposits of calcium in the basal ganglia and cerebral cortex of the brain. The gene that is responsible for Fahr syndrome has been mapped to chromosome 14. There is no cure for Fahr syndrome. Also called idiopathic basal ganglia calcification. Treatment is directed toward relieving symptoms.
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"Fahr syndrome" shown in the following materials:
Brain unable to localise tooth pain by Claudia Salwiczek, DTI ERLANGEN/LEIPZIG, Germany: The brain is not able to discriminate between a painful upper tooth and a painful lower tooth, researchers found. The[...]

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