Familial Idiopathic Basal Ganglia Calcification
It is possible that the main title of the report Familial Idiopathic Basal Ganglia Calcification is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report.
- Fahr disease, formerly
- striopallidodentate calcinosis
- cerebrovascular ferrocalcinosis
Familial idiopathic basal ganglia calcification (FIBGC) is a rare neurological disorder characterized by the presence of abnormal calcium deposits (calcifications) of unknown cause. Associated symptoms include progressive deterioration of cognitive abilities (dementia), loss of contact with reality (psychosis), mood swings and loss of acquired motor skills. As the condition progresses, paralysis may develop that is associated with increased muscle stiffness (rigidity) and restricted movements (spastic paralysis). Additional abnormalities may include relatively slow, involuntary, continual writhing movements (athetosis) or chorea, a related condition characterized by irregular, rapid, jerky movements.
WE MOVE (Worldwide Education and Awareness for Movement Disorders)
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NIH/National Institute of Neurological Disorders and Stroke
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MUMS National Parent-to-Parent Network
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Genetic and Rare Diseases (GARD) Information Center
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