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Primary progressive aphasia: a clinical approach

The primary progressive aphasias are a heterogeneous group of focal ‘language-led’ dementias that pose substantial challenges for diagnosis and management. Here we present a clinical approach to the progressive aphasias, based on our experience of these disorders and directed at non-specialists. We...

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Detalles Bibliográficos
Autores principales: Marshall, Charles R., Hardy, Chris J. D., Volkmer, Anna, Russell, Lucy L., Bond, Rebecca L., Fletcher, Phillip D., Clark, Camilla N., Mummery, Catherine J., Schott, Jonathan M., Rossor, Martin N., Fox, Nick C., Crutch, Sebastian J., Rohrer, Jonathan D., Warren, Jason D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5990560/
https://www.ncbi.nlm.nih.gov/pubmed/29392464
http://dx.doi.org/10.1007/s00415-018-8762-6
Descripción
Sumario:The primary progressive aphasias are a heterogeneous group of focal ‘language-led’ dementias that pose substantial challenges for diagnosis and management. Here we present a clinical approach to the progressive aphasias, based on our experience of these disorders and directed at non-specialists. We first outline a framework for assessing language, tailored to the common presentations of progressive aphasia. We then consider the defining features of the canonical progressive nonfluent, semantic and logopenic aphasic syndromes, including ‘clinical pearls’ that we have found diagnostically useful and neuroanatomical and other key associations of each syndrome. We review potential diagnostic pitfalls and problematic presentations not well captured by conventional classifications and propose a diagnostic ‘roadmap’. After outlining principles of management, we conclude with a prospect for future progress in these diseases, emphasising generic information processing deficits and novel pathophysiological biomarkers. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00415-018-8762-6) contains supplementary material, which is available to authorized users.