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Int Psychogeriatr ; 24(7): 1183-5, 2012 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-22436171

RESUMEN

Sporadic Creutzfeldt-Jakob disease (sCJD) is a rare and devastating illness. It is the most frequently encountered form of the spongiform encephalopathies with 50 new cases a year in the UK. It presents with a myriad of symptoms reflecting central nervous system dysfunction and is characterized by a rapidly progressive dementia leading to death. The disease process can pose multiple challenges: diagnostic conundrums, complexities in management, and palliative care issues. Good coordinated care between services and information is paramount in adequate management and delivery of care for patients suffering from sCJD.Psychiatry services frequently become involved in the assessment and management of sCJD.


Asunto(s)
Síndrome de Creutzfeldt-Jakob/diagnóstico , Anciano , Encéfalo/patología , Síndrome de Creutzfeldt-Jakob/patología , Síndrome de Creutzfeldt-Jakob/psicología , Diagnóstico Diferencial , Femenino , Humanos , Imagen por Resonancia Magnética , Masculino
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