A large pedigree with early-onset Alzheimer's disease: clinical, neuropathologic, and genetic characterization

Neurology. 1995 Jan;45(1):80-5. doi: 10.1212/wnl.45.1.80.

Abstract

We present clinical, neuropsychological, and neuropathologic data on a large pedigree including 34 subjects with early-onset progressive dementia. The mean (+/- SD) age at onset was 46 +/- 3.5 years and the mean age at death 52.6 +/- 5.7 years. Twelve patients were clinically diagnosed as having probable Alzheimer's disease (AD) according to the NINCDS-ADRDA criteria. Neuropsychological evaluation, performed at a moderate stage of the disease, was available in six subjects and showed a classic pattern of cognitive deficit. Myoclonus and extrapyramidal signs were common, and seizures were present in all affected subjects. There were neuropathologic changes typical of AD in two brains. A significant lod score of 5.48 was observed at a recombination fraction of theta = 0.0 with the genetic marker D14S43, thereby establishing that the responsible gene was located on chromosome 14q24.3. These results suggest that epilepsy could represent a particular feature in AD families linked to chromosome 14q.

Publication types

  • Case Reports
  • Clinical Trial
  • Comparative Study
  • Controlled Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Age of Onset
  • Alzheimer Disease / genetics*
  • Alzheimer Disease / pathology*
  • Alzheimer Disease / physiopathology
  • Brain / pathology*
  • Chromosome Mapping
  • Chromosomes, Human, Pair 14*
  • DNA / blood
  • Female
  • Genetic Linkage
  • Genetic Markers
  • Humans
  • Leukocytes / metabolism
  • Male
  • Middle Aged
  • Neurofibrillary Tangles / pathology
  • Neuropsychological Tests
  • Pedigree
  • Polymerase Chain Reaction
  • Reference Values
  • Sex Characteristics
  • Sex Factors

Substances

  • Genetic Markers
  • DNA