Pick and Alzheimer Diseases: A Rare Comorbidity Presenting as Corticobasal Syndrome

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F13%3A10191099" target="_blank" >RIV/00216208:11110/13:10191099 - isvavai.cz</a>

Nalezeny alternativní kódy

RIV/00216208:11210/13:10191099 RIV/00216208:11150/13:10191099 RIV/00064190:_____/13:#0000585 RIV/00064165:_____/13:10191099

Výsledek na webu

<a href="http://dx.doi.org/10.1097/WNN.0000000000000011" target="_blank" >http://dx.doi.org/10.1097/WNN.0000000000000011</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1097/WNN.0000000000000011" target="_blank" >10.1097/WNN.0000000000000011</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Pick and Alzheimer Diseases: A Rare Comorbidity Presenting as Corticobasal Syndrome

Popis výsledku v původním jazyce

We describe a patient with corticobasal syndrome in whom neuropathological examination on autopsy revealed Pick and Alzheimer diseases in comorbidity. Corticobasal degeneration is a tauopathy usually associated with asymmetric parkinsonism, parietal lobeinvolvement, and cognitive impairment. Corticobasal syndrome is the clinical presentation of corticobasal degeneration without neuropathological confirmation. A 66-year-old right-handed man slowly developed speech difficulties, right-hand clumsiness, and forgetfulness. His speech apraxia progressed to mutism with preserved comprehension, and his clumsiness progressed to severe apraxia involving both hands. He developed behavioral changes and severe amnesia. All of these features were consistent with corticobasal syndrome. His loss of episodic, verbal, and visuospatial memory suggested Alzheimer disease; however, beyond his frontotemporal neuropsychological profile, he had few symptoms characteristic of frontal lobe dementia. Magnetic r

Název v anglickém jazyce

Pick and Alzheimer Diseases: A Rare Comorbidity Presenting as Corticobasal Syndrome

Popis výsledku anglicky

We describe a patient with corticobasal syndrome in whom neuropathological examination on autopsy revealed Pick and Alzheimer diseases in comorbidity. Corticobasal degeneration is a tauopathy usually associated with asymmetric parkinsonism, parietal lobeinvolvement, and cognitive impairment. Corticobasal syndrome is the clinical presentation of corticobasal degeneration without neuropathological confirmation. A 66-year-old right-handed man slowly developed speech difficulties, right-hand clumsiness, and forgetfulness. His speech apraxia progressed to mutism with preserved comprehension, and his clumsiness progressed to severe apraxia involving both hands. He developed behavioral changes and severe amnesia. All of these features were consistent with corticobasal syndrome. His loss of episodic, verbal, and visuospatial memory suggested Alzheimer disease; however, beyond his frontotemporal neuropsychological profile, he had few symptoms characteristic of frontal lobe dementia. Magnetic r

Druh

J_x - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)

CEP obor

FH - Neurologie, neurochirurgie, neurovědy

OECD FORD obor

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Projekt

<a href="/cs/project/NT12094" target="_blank" >NT12094: Multidisciplinární přístup v diagnostice frontotemporálních lobárních degenerací a tauopatií: komplexní pohled na patogenetické mechanismy</a><br>

Návaznosti

Z - Vyzkumny zamer (s odkazem do CEZ)<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Rok uplatnění

2013

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Cognitive and Behavioral Neurology

ISSN

1543-3633

e-ISSN

—

Svazek periodika

26

Číslo periodika v rámci svazku

4

Stát vydavatele periodika

US - Spojené státy americké

Počet stran výsledku

6

Strana od-do

189-194

Kód UT WoS článku

000329188900003

EID výsledku v databázi Scopus

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