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Fahr syndrome: Difference between revisions
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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 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|G23.8 | |||
{{disease|Fahr|G23.8}} | |||
<ref>http://apps.who.int/classifications/icd10/browse/2015/en#/G23.8</ref> | <ref>http://apps.who.int/classifications/icd10/browse/2015/en#/G23.8</ref> | ||
==Links== | ==Links== | ||
Revision as of 18:16, 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
