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Fahr syndrome
The Fahr syndrome, is a rare neurological disease characterized by calcified deposits[1]
Disease classification WHO
Fahr G23.8
Links
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Saleem et al. Orphanet Journal of Rare Diseases 2013, 8:156
- Syndrome de Fahr : une complication rare de la radiothérapie cérébrale survenant chez un patient acromégale
- 原因遺伝子からみたパーキンソニズムを呈する疾患とその治療戦略
- Mushtaq R, Shoib S, M Raju, Naphade N, Shah T, Pawar A. Neuropsychiatric manifestations of Fahr's disease pathogenesis and potential for treatment. Ind Psiquiatría J [on line serie] 2013 [cited 24th august 2015]; 22: 153-4. See at: http://www.industrialpsychiatry.org/text.asp?2013/22/2/153/132931