Neuroinflammatory Pathways in the ALS-FTD Continuum: A Focus on Genetic Variants.
amyotrophic lateral sclerosis
autoimmune
frontotemporal dementia
genetic
immune system
neuroinflammation
therapy
Journal
Genes
ISSN: 2073-4425
Titre abrégé: Genes (Basel)
Pays: Switzerland
ID NLM: 101551097
Informations de publication
Date de publication:
21 08 2023
21 08 2023
Historique:
received:
15
07
2023
revised:
18
08
2023
accepted:
18
08
2023
medline:
28
8
2023
pubmed:
26
8
2023
entrez:
26
8
2023
Statut:
epublish
Résumé
Amyotrophic Lateral Sclerosis (ALS) and Frontotemporal dementia (FDT) are progressive neurodegenerative disorders that, in several cases, overlap in clinical presentation, and genetic and pathological disease mechanisms. About 10-15% of ALS cases and up to 40% of FTD are familial, usually with dominant traits. ALS and FTD, in several cases, share common gene mutations, such as in
Identifiants
pubmed: 37628709
pii: genes14081658
doi: 10.3390/genes14081658
pmc: PMC10454262
pii:
doi:
Substances chimiques
CHCHD10 protein, human
0
Mitochondrial Proteins
0
Types de publication
Journal Article
Review
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
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