2015
DOI: 10.5455/gmj-30-173253
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Creutzfeldt-Jakob disease presented with dizziness, weakness and neuropsychiatric symptoms: 2 Case Reports

Abstract: Creutzfeldt-Jakob disease (CJD) is among very rare, progressive, untreatable, neurodegenerative prion diseases. While the incidence is reported as 1/1000000 years in European countries, sporadic cases are rarely presented in Turkey. Clinical findings are in the form of rapid progressive dementia, myoclonus, cerebellar, pyramidal and extra pyramidal symptoms. Definitive diagnosis is established by histopathological examination. Our case is a 64-year-old male and 70-year-old female patients admitted with dizzine… Show more

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Cited by 2 publications
(3 citation statements)
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“…Differential diagnosis of patients should be conducted properly. Temporal arthritis, HIV, Legionella infections and slow virus infections may be mistaken for viral encephalitis, particularly in cases involving stroke and optic nerves [5,6,7]. At first, aneurysm operation, ptosis, and seizure in the medical history of our patient suggested a new cerebrovascular attack.…”
Section: Discussionmentioning
confidence: 77%
“…Differential diagnosis of patients should be conducted properly. Temporal arthritis, HIV, Legionella infections and slow virus infections may be mistaken for viral encephalitis, particularly in cases involving stroke and optic nerves [5,6,7]. At first, aneurysm operation, ptosis, and seizure in the medical history of our patient suggested a new cerebrovascular attack.…”
Section: Discussionmentioning
confidence: 77%
“…Although definitive diagnosis is made from brain biopsy, this is not always an easy method to apply (1,11,12).…”
Section: Discussionmentioning
confidence: 99%
“…Following the onset of symptoms, mean life expectancy is up to 1 year. In the early stages of CJD, depressive symptoms such as fatigue, apathy, withdrawal, sleep and eating disorders and personality changes may be seen in approximately 1 in 3 patients (1)(2)(3)(4).…”
Section: Introductionmentioning
confidence: 99%