La encefalopatía espongiforme: ¿un trastorno conversivo?

  • Meca García J
  • Fernández-Miranda López S
  • Collado Rueda F
  • et al.
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Abstract

Prionpathies represent a group of neurodegenerative diseases of familiar, sporadic or acquired origin, heterogeneous symptoms and fatal outcome. The psychiatric symptoms can be present at the beginning and/or during the clinical evolution, with the presence or not of neurological disorders. Patients with these sympthoms are referred to psychiatric units, both at hospital level and as outpatients, to study a psychiatric disorder. In the described clinical case, the patieht was admitted several times at emergency units, rated by neurologists and psychiatrists leading to different psychiatric disorders diagnoses. However spongiform encephalopathy was diagnosed only during the last month of the disease. (English) [ABSTRACT FROM AUTHOR]

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APA

Meca García, J. M., Fernández-Miranda López, S., Collado Rueda, F., & Vázquez Gutiérrez, F. (2014). La encefalopatía espongiforme: ¿un trastorno conversivo? Revista de La Asociación Española de Neuropsiquiatría, 34(124), 785–789. https://doi.org/10.4321/s0211-57352014000400010

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