Significats de wilhemsen-lynch disease en anglès

Recent research on frontotemporal dementia highlights the potential value of these approaches.

Results: The frontotemporal dementia subgroup represented approximately half of all FTLD diagnoses.

Other diseases which may involve tau deposition include frontotemporal dementia and corticobasal degeneration.

Neuroimaging features were consistent with the diagnosis of frontotemporal dementia.

The authors conclude that PSEN1 mutations can be associated with clinical features of frontotemporal dementia.

Methods: Electronic databases were searched using terms related to frontotemporal lobar degeneration and movement disorders.

Mutations in the gene encoding PGRN give rise to shortage of PGRN and cause familial frontotemporal lobar degeneration.

Summary: This represents the first systematic review and meta-analysis of the occurrence of movement disorder phenomenology in genetic frontotemporal lobar degeneration.

These findings further highlight that plasma PGRN levels may not accurately predict clinical features or response to future frontotemporal lobar degeneration therapies.

Mutations in various RBPs cause several diseases of the central nervous system, including frontotemporal lobar degeneration, amyotrophic lateral sclerosis and fragile X syndrome.