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Genetic investigation of dementias in clinical practice

BACKGROUND: The field of neurodegenerative dementia genetics has advanced significantly over the past two decades, but there are still more to be discovered (such as the gene mutation in some familial forms of dementia). OBJECTIVE: to provide a brief review of the most recent discoveries regarding m...

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Detalles Bibliográficos
Autor principal: Takada, Leonel Tadao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academia Brasileira de Neurologia - ABNEURO 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9491423/
https://www.ncbi.nlm.nih.gov/pubmed/35976293
http://dx.doi.org/10.1590/0004-282X-ANP-2022-S103
Descripción
Sumario:BACKGROUND: The field of neurodegenerative dementia genetics has advanced significantly over the past two decades, but there are still more to be discovered (such as the gene mutation in some familial forms of dementia). OBJECTIVE: to provide a brief review of the most recent discoveries regarding monogenic dementia, and covering the most frequent genetic diseases that can cause dementia (neurodegenerative or not). METHODS: a review of the literature will be carried out. RESULTS: neurodegenerative dementias, vascular dementias and leukoencephalopathies caused by single pathogenic variants are presented. CONCLUSION: The spectrum of clinical presentations for most of the genes discussed is wide, and hence genetic testing in clinic should try to cover as many genes as possible.