Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Slowly progressive behavioral frontotemporal dementia with C9orf72 mutation. Case report and review of the literature.

Neurocase - 1 Feb 2018

Llamas-Velasco S, García-Redondo A, Herrero-San Martín A, Puertas Martín V, González-Sánchez M, Pérez-Martínez D A, Villarejo-Galende A

Abstract excerpt

We present a 86-year-old woman without relevant medical history and two brothers who died by dementia, who started at 55 years with depression and personality changes with ongoing worsening (>30 years) and functional decline. Screening dementia blood test and brain magnetic resonance imaging did not show results that pointed to a secondary cause. The patient met the diagnostic criteria for possible behavioral...

Topics

Join the communities discussing this publication.

Aged, 80 and over
C9orf72 Protein
Disease Progression
Frontotemporal Dementia
Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 29355451
DOI: 10.1080/13554794.2018.1428353

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Slowly progressive behavioral frontotemporal dementia with C9orf72 mutation. Case report and review of the literature.PMID 29355451Read ↗

Atypical, slowly progressive behavioural variant frontotemporal dementia associated with C9ORF72 hexanucleotide expansion.Semantic proximity Read ↗

Rapidly progressive dementia with psychotic onset in a patient with the C9ORF72 mutation.Semantic proximity Read ↗

Familial benign frontotemporal deterioration with C9ORF72 hexanucleotide expansion.Semantic proximity Read ↗

Early onset frontotemporal dementia with psychiatric presentation due to the C9ORF72 hexanucleotide repeat expansion: a case report.Semantic proximity Read ↗

Frontotemporal dementia associated with the C9ORF72 mutation: a unique clinical profile.Semantic proximity Read ↗

Frontotemporal dementia in a Brazilian kindred with the c9orf72 mutation.Semantic proximity Read ↗

[Genetics of frontotemporal dementia].Semantic proximity Read ↗

The behavioural variant frontotemporal dementia phenocopy syndrome is a distinct entity - evidence from a longitudinal study.Semantic proximity Read ↗

Distinct clinical characteristics of C9orf72 expansion carriers compared with GRN, MAPT, and nonmutation carriers in a Flanders-Belgian FTLD cohort.Semantic proximity Read ↗

Clinical heterogeneity of the C9orf72 genetic mutation in frontotemporal dementia.Semantic proximity Read ↗

Frontotemporal dementia with psychosis, parkinsonism, visuo-spatial dysfunction, upper motor neuron involvement associated to expansion of C9ORF72: a peculiar phenotype?Semantic proximity Read ↗

Familial Lund frontotemporal dementia caused by C9ORF72 hexanucleotide expansion.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.