SwePub
Sök i LIBRIS databas

  Extended search

WFRF:(Johannsen T.)
 

Search: WFRF:(Johannsen T.) > (2000-2004) > Chromosome 3 linked...

  • Gydesen, S (author)

Chromosome 3 linked frontotemporal dementia (FTD-3)

  • Article/chapterEnglish2002

Publisher, publication year, extent ...

  • 2002

Numbers

  • LIBRIS-ID:oai:lup.lub.lu.se:8e88a36e-2e27-4440-b36a-da2597ecabb4
  • https://lup.lub.lu.se/record/323371URI

Supplementary language notes

  • Language:English
  • Summary in:English

Part of subdatabase

Classification

  • Subject category:art swepub-publicationtype
  • Subject category:ref swepub-contenttype

Notes

  • Background: The authors have identified and studied a large kindred in which frontotemporal dementia (FTD) is inherited as an autosomal dominant trait. The trait has been mapped to the pericentromeric region of chromosome 3. Methods: The authors report on the clinical, neuroimaging, neuropsychological, and pathologic features in this unique pedigree collected during 17 years of study. Results: Twenty-two individuals in three generations have been affected; the age at onset varies between 46 and 65 years. The disease presents with a predominantly frontal lobe syndrome but there is also evidence for temporal and dominant parietal lobe dysfunction. Late in the illness individuals develop a florid motor syndrome with pyramidal and extrapyramidal features. Structural imaging reveals generalized cerebral atrophy; H-2 O-15-PET scanning in two individuals relatively early and late in the disease shows a striking global reduction in cerebral blood flow affecting all lobes. On macroscopic pathologic examination, there is generalized cerebral atrophy affecting the frontal lobes preferentially. Microscopically, there is neuronal loss and gliosis without specific histopathologic features. Conclusions: FTD-3 shares clinical and pathologic features with other forms of FTD and fulfills international consensus criteria for FTD. There is involvement of the parietal lobes clinically, radiologically, and pathologically in FTD-3 in contrast to some forms of FTD. This more diffuse involvement of the cerebral cortex leads to a distinctive, global pattern of reduced blood flow on PET scanning.

Subject headings and genre

Added entries (persons, corporate bodies, meetings, titles ...)

  • Brown, JM (author)
  • Brun, ArneLund University,Lunds universitet,Tumörmikromiljö,Sektion I,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Tumor microenvironment,Section I,Department of Clinical Sciences, Lund,Faculty of Medicine(Swepub:lu)pat-ab8 (author)
  • Chakrabarti, L (author)
  • Gade, A (author)
  • Johannsen, P (author)
  • Rossor, M (author)
  • Thusgaard, T (author)
  • Grove, A (author)
  • Yancopoulou, D (author)
  • Spillantini, MG (author)
  • Fisher, EMC (author)
  • Collinge, J (author)
  • Sorensen, SA (author)
  • TumörmikromiljöSektion I (creator_code:org_t)

Related titles

  • In:Neurology59:10, s. 1585-15941526-632X

Internet link

Find in a library

  • Neurology (Search for host publication in LIBRIS)

To the university's database

Search outside SwePub

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Close

Copy and save the link in order to return to this view