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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 [[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}} | ||
<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== | ||
[http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4485651/pdf/amjcaserep-16-382.pdf Quantitative MR Markers and Psychiatric Symptoms in a Patient with Fahr Disease] | *[http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4485651/pdf/amjcaserep-16-382.pdf Quantitative MR Markers and Psychiatric Symptoms in a Patient with Fahr Disease] | ||
<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] | *[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] | ||
*[https://www.jstage.jst.go.jp/article/yakushi/134/12/134_14-00209-3/_pdf 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 | |||
{{Wikidata|Q1947307}} as basal ganglia calcification | |||
{{refs}} | |||
[[Category:Disease]] | [[Category:Disease]] | ||
[[nl:Fahr-Syndrom]] | |||
Latest revision as of 22:57, 26 February 2019
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
as basal ganglia calcification
| References: |