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Fahr syndrome: Difference between revisions
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<gallery>File: Fahr cc.png|Saleem et al. Orphanet Journal of Rare Diseases 2013, 8:156</gallery> | <gallery>File: Fahr cc.png|Saleem et al. Orphanet Journal of Rare Diseases 2013, 8:156</gallery> | ||
[http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4247864/pdf/PAMJ-18-287.pdf Syndrome de Fahr : une complication rare de la radiothérapie cérébrale survenant chez un patient acromégale] | |||
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[[Category:Disease]] | [[Category:Disease]] | ||
Revision as of 18:22, 24 August 2015
The Fahr syndrome, is a rare neurological disease characterized by calcified deposits[1]
Disease classification WHO
Fahr G23.8
Links
Quantitative MR Markers and Psychiatric Symptoms in a Patient with Fahr Disease
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Saleem et al. Orphanet Journal of Rare Diseases 2013, 8:156
