Creutzfeldt‐Jakob disease with neuroleptic malignant syndrome [PDF]
Clinical Case Reports, 2021 Creutzfeldt‐Jakob disease (CJD) is a rare rapidly progressive fatal neurodegenerative disease. Neuroleptic malignant syndrome (NMS) is a complication of antipsychotic medications which may be used to treat neuropsychiatric symptoms of CJD.
Julija Čiauškaitė +5 more
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Sporadic Creutzfeldt-Jakob Syndrome Misdiagnosed as Recurrent Stroke: A Case Report [PDF]
Annals of Geriatric Medicine and Research, 2021 While sporadic Creutzfeldt-Jakob disease (sCJD) typically presents with neurological symptoms such as cognitive impairment, ataxia, and myoclonus, its clinical manifestations can be diverse.
Min Joon Bae +3 more
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Alice in Wonderland Syndrome as a Presenting Manifestation of Creutzfeldt-Jakob Disease [PDF]
Frontiers in Neurology, 2019 Background: Alice in Wonderland syndrome (AIWS) is a rare neurological disorder characterized by distortions of visual perception (metamorphopsias), the body image, and the experience of time, along with derealization and depersonalization.
Tirza Naarden +6 more
doaj +5 more sources
Alice in wonderland syndrome as a manifestation of Creutzfeldt-Jakob disease
Annals of Indian Academy of Neurology, 2023 Shweta Pandey +3 more
doaj +4 more sources
An Atypical Case of Creutzfeldt-Jakob Syndrome Presenting with Cacosmia and Amyloid Positivity [PDF]
Journal of Alzheimer's Disease ReportsThis report presents a challenging case of Creutzfeldt-Jakob Disease (CJD), a rare and rapidly progressing neurological disorder. The patient exhibited diverse and progressive neuro-psychiatric symptoms, including memory impairment, behavioral changes ...
Alfredo Gabriele Nanni +9 more
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Creutzfeldt–Jakob Disease: An Unusual Presentation of Corticobasal Syndrome [PDF]
Cureus, 2020 Corticobasal syndrome is an atypical parkinsonian syndrome consisting of a constellation of clinical findings that can be the result of various etiologies. While most cases are a result of a tauopathy, such as corticobasal degeneration, other etiologies must be considered in the evaluation of patients presenting with corticobasal syndrome. We present a
Gosden, Grant P +3 more
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CREUTZFELDT-JAKOB SYNDROME OF GENETIC ORIGIN: SERIES OF CASES IN THE ARGENTINIAN PATAGONIA [PDF]
BAG. Journal of Basic and Applied Genetics, 2020 Creutzfeldt-Jakob disease (CJD) is an uncommon neurodegenerative disorder with an incidence of 1 per 1,000,000 in humans per year, typically characterized by rapidly progressive dementia, ataxia, myoclonus and behavioral changes.
Exeni Díaz G. +3 more
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Creutzfeldt-Jakob Disease Presenting as Posterior Reversible Encephalopathy Syndrome [PDF]
Cureus, 2020 Creutzfeldt-Jakob disease (CJD) is the most common human prion disease presenting with subacute cognitive decline. Common MRI findings for CJD include the T2 prolongation signal of the putamen and head of caudate. Diffusion-weighted MRI (DW-MRI) is considered to be the most sensitive technique for the detection of CJD-related abnormalities, especially ...
Bittar, Jan +4 more
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Systematic review of pharmacological management in Creutzfeldt-Jakob disease: no options so far?
Arquivos de Neuro-Psiquiatria, 2022 Background The Creutzfeldt-Jakob disease (CJD) is a spongiform encephalopathy that manifests as a rapidly progressive dementia syndrome. Currently, CJD has no cure, and many patients die within the first year, but some drugs are being studied ...
Luiz Henrique Lélis Miranda +9 more
doaj +2 more sources
Frontiers in Neurology, 2022 The relationship between severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and neurodegenerative diseases is yet to be fully clarified.
Gabriela Almeida Pimentel +3 more
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