Creutzfeldt-Jacob Disease with presence of psychomotor agitation

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Creutzfeldt-Jacob Disease: a case report

Creutzfeldt-Jacob disease is a rare, neurodegenerative disease caused by a prion protein. The patients are usually between 40 and 60 years old. Most of the patients die within one year after onset of the disease. A typical case is reported. It is pointed out that such a dramatic development can cause anxiety and a feeling of inadequacy for close relatives. To avoid adverse consequences, it is i...

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creutzfeldt-jacob disease: a case report.

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Creutzfeldt-Jacob Disease with psychiatric onset: a case report Malattia di Creutzfeldt-Jacob con presentazione psichiatrica: un caso clinico

Case report We describe the case of an elderly female patient who presented with psychotic symptoms in the absence of neurological signs and symptoms, and after systematic diagnostic evaluation eventually turned out to be a sporadic CJD case. Conclusions In clinical practice CJD should not be neglected as differential diagnosis in elderly patients with negative psychiatric history referring to ...

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Sporadic Creutzfeldt-Jacob disease (sCJD) usually presents with typical clinical signs. Prodromal symptoms lasting for several weeks are followed by dementia, myoclonus, ataxia and abnormalities of vision (1). Supranuclear gaze palsies accompanying sCJD have rarely been reported. Some of these reported cases were initially diagnosed as progressive supranuclear palsy (PSP) and the diagnosis was ...

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ژورنال

عنوان ژورنال: Dusunen Adam: The Journal of Psychiatry and Neurological Sciences

سال: 2018

ISSN: 1018-8681,1309-5749

DOI: 10.5350/dajpn2018310113