Wikisage, the free encyclopedia of the second generation, is digital heritage
Fahr syndrome: Difference between revisions
Jump to navigation
Jump to search
m (eng) |
mNo edit summary |
||
| Line 1: | Line 1: | ||
The Fahr syndrome, is a rare neurological disease characterized by calcified deposits<ref>[http://www.ojrd.com/content/pdf/1750-1172-8-156.pdf Fahr’s syndrome: literature review of current evidence] </ref> | The [[Karl_Theodor_Fahr|Fahr syndrome]], is a rare neurological disease characterized by calcified deposits<ref>[http://www.ojrd.com/content/pdf/1750-1172-8-156.pdf Fahr’s syndrome: literature review of current evidence] </ref> | ||
{{disease|Fahr|G23.8}} | {{disease|Fahr|G23.8}} | ||
| Line 15: | Line 15: | ||
[[Category:Disease]] | [[Category:Disease]] | ||
[[nl:Fahr-Syndrom]] | [[nl:Fahr-Syndrom]] | ||
Revision as of 22:26, 14 April 2017
The Fahr syndrome, is a rare neurological disease characterized by calcified deposits[1]
Disease classification WHO
Fahr G23.8
Links
-
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