Syndrome Fahr: Neurologic manifestation of endocrine disease
Syndrome Fahr is described as calcification of the basal ganglia and is a rare inherited or sporadic neurological disease with a prevalence of 1:1000000 (1). For the first time described in 1930 in the works of Dr. Karl Theodor Fahr, it is characterized by calcium deposition in areas of the brain to...
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| Principais autores: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Specijalna bolnica za bolesti štitaste žlezde i bolesti metabolizma Zlatibor
2020-01-01
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| Series: | Medicinski Glasnik Specijalne Bolnice za Bolesti Štitaste Žlezde i Bolesti Metabolizma "Zlatibor" |
| Acceso en liña: | https://scindeks-clanci.ceon.rs/data/pdf/1821-1925/2020/1821-19252077057M.pdf |
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