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Talk:Frontotemporal dementia

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Life Expectancy

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Did I miss it? I can't find anything on life expectancy in the article.

Its in prognosis. 2-20 years Sawerchessread (talk) 16:47, 5 January 2024 (UTC)[reply]

Please

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Please go to www.ftd-picks.org for further information about frontotemporal dementia from the Association for FrontoTemporal Dementia (AFTD) and links to face-to-face and online support groups for FTD caregivers.

Far more sources - far more excellent sources, including some really good and more recent research published in refereed journals, and synopsized in popular lay and scientific press - can be found than the one or two mentioned in this article. MaynardClark (talk) 19:23, 5 October 2017 (UTC)[reply]

MND is not only ALS

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"FTD can occur in patients with motor neurone disease (also known in the US as Lou Gehrig's disease or amyotrophic lateral sclerosis) in a small number of cases."

As I understand, MND includes ALS, but also other diseases. So the sentence should read "In a small number of cases, FTD can occur in patients with motor neuron diseases such as amyotrophic lateral sclerosis (also known as Lou Gehrig's disease in the US)." -Pgan002 18:53, 15 August 2007 (UTC)[reply]

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The official external links policy does not allow the inclusion of internet chat boards, patient support groups, or related links in the article. External links need to be encyclopedic in nature. WhatamIdoing (talk) 01:52, 10 April 2008 (UTC)[reply]

Refs

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Some unsourced statements in this article may have come from any of the following list of original references:

  • Neary D, Snowden JS, Gustafson L; et al. (1998). "Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria". Neurology. 51 (6): 1546–54. PMID 9855500. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
  • Hodges JR, Patterson K, Oxbury S, Funnell E (1992). "Semantic dementia: progressive fluent aphasia with temporal lobe atrophy". Brain. 115 (6): 1783–806. PMID 1486461.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  • Neary D, Snowden JS, Mann DM (2000). "Classification and description of frontotemporal dementias". Ann. N. Y. Acad. Sci. 920: 46–51. PMID 11193176.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  • Kramer JH, Jurik J, Sha SJ; et al. (2003). "Distinctive neuropsychological patterns in frontotemporal dementia, semantic dementia, and Alzheimer disease". Cogn Behav Neurol. 16 (4): 211–8. PMID 14665820. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
  • Rosen HJ, Gorno-Tempini ML, Goldman WP; et al. (2002). "Patterns of brain atrophy in frontotemporal dementia and semantic dementia". Neurology. 58 (2): 198–208. PMID 11805245. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
  • Miller BL, Seeley WW, Mychack P, Rosen HJ, Mena I, Boone K (2001). "Neuroanatomy of the self: evidence from patients with frontotemporal dementia". Neurology. 57 (5): 817–21. PMID 11552010.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  • Diehl J, Ernst J, Krapp S, Förstl H, Nedopil N, Kurz A (2006). "[Misdemeanor in frontotemporal dementia]". Fortschr Neurol Psychiatr (in German). 74 (4): 203–10. PMID 16671160.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  • Seeley WW, Carlin DA, Allman JM; et al. (2006). "Early frontotemporal dementia targets neurons unique to apes and humans". Ann. Neurol. 60 (6): 660–7. doi:10.1002/ana.21055. PMID 17187353. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
  • Hodges JR, Davies R, Xuereb J, Kril J, Halliday G (2003). "Survival in frontotemporal dementia". Neurology. 61 (6): 349–354. PMID 12913196.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  • Hodges JR, Davies R, Xuereb J, Casey B, Broe M, Bak T, Kril J, Halliday G (2004). "Clinicopathological correlates in frontotemporal dementia". Ann. Neurol. 56 (3): 349–354. doi:10.1002/ana.20203. PMID 15349867.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  • Mioshi E, Kipps C, Dawson K. Mitchell J, Graham A, Hodges JR (2007). "Activities of daily living in frontotemporal dementia". Neurology. 68: 2077–2084. doi:10.1212/01.wnl.0000264897.13722.53. PMID 17562828.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  • Mendez MF, Shapira JS, Woods RJ, Licht EA, Saul RE Jr (2008). "Psychotic symptoms in frontotemporal dementia: prevalence and review". Dement Geriatr Cogn Disord. 25 (3): 206–211.{{cite journal}}: CS1 maint: multiple names: authors list (link)

Please feel free to move these refs into the article if you know which ones belong to which statements. WhatamIdoing (talk) 02:05, 24 March 2009 (UTC)[reply]

What about a better definition?

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I think that this defintion may fit better.

"Frontotemporal dementia (FTD) is a neurodegenerative disorder characterized by progressive deterioration of behaviour, personality and language abilities in association with prominent frontal and temporal lobar atrophy."

Moreover it is referenced ==> Graham A & Hodges J.R. Psichiatry. 2007;7:24-8 — Preceding unsigned comment added by 151.66.93.48 (talk) 08:17, 8 April 2013 (UTC)[reply]

It is a really good definition, but ideally, a definition should not be a quote. However, I won't remove it if you make the edit. Please provide full source information though (name of article), and make sure you spell correctly. Lova Falk talk 10:41, 19 April 2013 (UTC)[reply]

stroop task

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the stroop task is used to specifically assess orbitofrontal dysfunction. it has a remarkable specificity and is used in cerebral perfusion studies to bias perfusion in the orbitofrontal lobe. persistent hypoperfusion can be understood to prove orbitofrontal dysfunction. there are sources available that suggest its utility in the early diagnosis of frontotemporal dementia via this symptom as the early stages can consist of degeneration progressing from the orbitofrontal lobe. http://www.ncbi.nlm.nih.gov/pubmed/11320164 http://memory.ucsf.edu/ftd/overview/biology/executive/single — Preceding unsigned comment added by 118.208.238.12 (talk) 15:49, 15 August 2014 (UTC)[reply]

Costs - Socieconomic Burden of FTD

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Some members of the Association for Frontotemporal Degeneration (AFD), http://www.theaftd.org/ researched the socieconomic burden of FTD[1][2][3] and concluded that "frontotemporal degeneration (FTD) accounts for 20 to 50 percent of dementia cases in people under the age of 65."

References

  1. ^ Newsroom: Florida Atlantic University. Study Reveals Staggering Economic Burden of Dementia in Younger People: First-of-its-kind Study on Frontotemporal Degeneration Led by FAU. Article ID: 682215. Released: 3-Oct-2017 4:30 PM EDT
  2. ^ Florida Atlantic University. Staggering economic burden of dementia in younger people, study reveals: First-of-its-kind study on frontotemporal degeneration. October 4, 2017
  3. ^ James E. Galvin, David H. Howard, Sharon S. Denny, Susan Dickinson, Nadine Tatton. The social and economic burden of frontotemporal degeneration. Neurology, 2017; 10.1212/WNL.0000000000004614 DOI: 10.1212/WNL.0000000000004614

Picks disease

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Why do we not give weight in the lede to Pick's disease as an altname here? Just dropping by as I read about it with an actor's diagnosis today. Thought this might have been discussed before, but if it hasn't the former and historic name would certainly be due (in my opinion). Thanks! Jtbobwaysf (talk) 02:18, 17 February 2023 (UTC)[reply]

Frequency

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Stats on incidence or prevalence are missing from the article; seems like a pretty basic fact. -- Beland (talk) 07:42, 12 February 2024 (UTC)[reply]

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