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Cognitive dysfunction in corticobasal degeneration / Disfunção cognitiva na degeneração corticobasal
Oliveira, Laís Machado de; Barcellos, Igor; Teive, Hélio A G; Munhoz, Renato Puppi.
  • Oliveira, Laís Machado de; University Health Network. Toronto Western Hospital. Morton and Gloria Shulman Movement Disorders Centre. Toronto. CA
  • Barcellos, Igor; University Health Network. Toronto Western Hospital. Morton and Gloria Shulman Movement Disorders Centre. Toronto. CA
  • Teive, Hélio A G; University Health Network. Toronto Western Hospital. Morton and Gloria Shulman Movement Disorders Centre. Toronto. CA
  • Munhoz, Renato Puppi; University Health Network. Toronto Western Hospital. Morton and Gloria Shulman Movement Disorders Centre. Toronto. CA
Arq. neuropsiquiatr ; 75(8): 570-579, Aug. 2017. tab, graf
Article Dans Anglais | LILACS | ID: biblio-888318
ABSTRACT
ABSTRACT Corticobasal degeneration (CBD) was originally described as a distinct clinicopathological entity in 1967. Since then, different phenotypic presentations have emerged as possible manifestations of CBD histopathological findings. In addition, pathophysiological findings and the molecular basis have been delineated and several aspects of its cognitive manifestations have been clarified. Thus, not only the spectrum of what is currently designated as CBD has expanded, but overlap with other degenerative and even secondary disorders has made clinical diagnostic certainty even more challenging in the absence of specific and readily-available markers. Cognitive deficits in CBD are now recognized as a frequent initial presentation and may appear up to eight years before the motor symptoms, depending on the phenotypic variant. Characteristic cognitive features of CBD involve language deficits, visuospatial and executive dysfunctions, apraxia, and behavioral disorders. Semantic and episodic memories are usually preserved, while language is often impaired in the early stages.
RESUMO
RESUMO A degeneração corticobasal (DCB) foi originalmente descrita como uma entidade clínico-patológica distinta em 1967. Desde então, nossa compreensão sobre DCB evoluiu substancialmente. Diferentes apresentações fenotípicas emergiram refletindo possíveis manifestações das anormalidades histopatológicos da DCB. Adicionalmente, dados fisiopatológicos e moleculares foram delineados e aspectos das manifestações cognitivas foram explorados. Assim, não só o espectro do que é atualmente designado DCB foi expandido, mas a sobreposição com outras doenças degenerativas e até mesmo secundárias tornaram o diagnóstico clínico ainda mais desafiador na ausência de marcadores específicos e prontamente disponíveis. Déficits cognitivos na DCB são agora reconhecidos frequentemente como apresentações iniciais e podem surgir até 8 anos antes dos sintomas motores, dependendo da variante fenotípica. O quadro cognitivo envolve característicamente déficits de linguagem, disfunção visuoespacial e executiva, apraxia, e distúrbios comportamentais. Anormalidades da linguagem são frequentemente descritas nos estágios iniciais da DCB.
Sujets)


Texte intégral: Disponible Indice: LILAS (Amériques) Sujet Principal: Noyaux gris centraux / Cortex cérébral / Maladies neurodégénératives / Démence / Dysfonctionnement cognitif Type d'étude: Etude diagnostique Limites du sujet: Humains langue: Anglais Texte intégral: Arq. neuropsiquiatr Thème du journal: Neurologie / Psychiatrie Année: 2017 Type: Article Pays d'affiliation: Canada Institution/Pays d'affiliation: University Health Network/CA

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Texte intégral: Disponible Indice: LILAS (Amériques) Sujet Principal: Noyaux gris centraux / Cortex cérébral / Maladies neurodégénératives / Démence / Dysfonctionnement cognitif Type d'étude: Etude diagnostique Limites du sujet: Humains langue: Anglais Texte intégral: Arq. neuropsiquiatr Thème du journal: Neurologie / Psychiatrie Année: 2017 Type: Article Pays d'affiliation: Canada Institution/Pays d'affiliation: University Health Network/CA