Searching map area
Frontotemporal lobar degeneration
? TBD
Atrophy of the brain's frontal and temporal lobes
Join to rate
Ratings
0
Nobody has rated this yet. Be the first!
Subclasses
1
GRN-related frontotemporal lobar degeneration with Tdp43 inclusions
Human disease
Subject of
10
Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration
scientific article
Behavioral variant frontotemporal lobar degeneration with amyotrophic lateral sclerosis with a chromosome 9p21 hexanucleotide repeat
scientific article published in 2012
Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar Degeneration
scientific article
From frontotemporal lobar degeneration pathology to frontotemporal lobar degeneration biomarkers.
scientific article published on April 2013
Atypical multiple system atrophy is a new subtype of frontotemporal lobar degeneration: frontotemporal lobar degeneration associated with α-synuclein.
scientific article published on 12 May 2015
Frontotemporal lobar degeneration with ubiquitin-positive, but TDP-43-negative inclusions
article published in 2008
Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update
scientific article
Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations
scientific article published on 11 January 2008
Genotype–phenotype links in frontotemporal lobar degeneration
scientific article published on 01 June 2018
TDP-43 pathologic lesions and clinical phenotype in frontotemporal lobar degeneration with ubiquitin-positive inclusions
scientific article published on 01 October 2007
Lists
0
Join to rate

Frontotemporal lobar degeneration (FTLD) is a pathological process that occurs in frontotemporal dementia. It is characterized by atrophy in the frontal lobe and temporal lobe of the brain, with sparing of the parietal and occipital lobes.

Instance of
designated intractable/rare disease
Rare disease
Disease
Signs and symptoms
Subclass of
Neurodegenerative disease
Wikidata