Literature DB >> 7205322

Familial Alzheimer's disease in two kindreds of the same geographic and ethnic origin. A clinical and genetic study.

J Goudsmit, B J White, L R Weitkamp, B J Keats, C H Morrow, D C Gajdusek.   

Abstract

Alzheimer's disease (AD) occurred in 37 individuals from two kindreds of Jewish ancestry with a mode of transmission suggesting an autosomal dominant genetic trait. Both kindreds originated from Byelorussia and spoke the Lithuanian dialect of Yiddish. In one of the two families one case of pathologically confirmed AD occurred with clinical and neuropathological signs of Parkinson's disease. In the other family one case of amyotrophic lateral sclerosis and one case of Down's syndrome occurred, both without clinical or pathological signs of AD. In the single kindred tested, a study of the chromosome 6 markers HLA, Bf and GLO failed to reveal a correlation between the transmission of AD and the segregation of these markers. The association of increased aneuploidy of peripheral blood chromosomes with AD was not confirmed in either of these families. Genetic differences between the familial and the sporadic form of AD are discussed.

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Year:  1981        PMID: 7205322     DOI: 10.1016/0022-510x(81)90190-8

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  10 in total

1.  Complement allotypes in familial and sporadic Alzheimer's disease.

Authors:  P K Panegyres; R L Dawkins
Journal:  J Neurol       Date:  1991-09       Impact factor: 4.849

Review 2.  Epigenomics of Alzheimer's disease.

Authors:  David A Bennett; Lei Yu; Jingyun Yang; Gyan P Srivastava; Cristin Aubin; Philip L De Jager
Journal:  Transl Res       Date:  2014-05-16       Impact factor: 7.012

3.  Alzheimer disease: evidence for susceptibility loci on chromosomes 6 and 14.

Authors:  L R Weitkamp; L Nee; B Keats; R J Polinsky; S Guttormsen
Journal:  Am J Hum Genet       Date:  1983-05       Impact factor: 11.025

4.  Racial differences in the etiology of dementia and frequency of Alzheimer lesions in the brain.

Authors:  S M de la Monte; G M Hutchins; G W Moore
Journal:  J Natl Med Assoc       Date:  1989-06       Impact factor: 1.798

5.  Lewy bodies contain altered alpha-synuclein in brains of many familial Alzheimer's disease patients with mutations in presenilin and amyloid precursor protein genes.

Authors:  C F Lippa; H Fujiwara; D M Mann; B Giasson; M Baba; M L Schmidt; L E Nee; B O'Connell; D A Pollen; P St George-Hyslop; B Ghetti; D Nochlin; T D Bird; N J Cairns; V M Lee; T Iwatsubo; J Q Trojanowski
Journal:  Am J Pathol       Date:  1998-11       Impact factor: 4.307

6.  Linkage and mutational analysis of familial Alzheimer disease kindreds for the APP gene region.

Authors:  K Kamino; H T Orr; H Payami; E M Wijsman; M E Alonso; S M Pulst; L Anderson; S O'dahl; E Nemens; J A White
Journal:  Am J Hum Genet       Date:  1992-11       Impact factor: 11.025

Review 7.  Genetic dissection of Alzheimer disease, a heterogeneous disorder.

Authors:  G D Schellenberg
Journal:  Proc Natl Acad Sci U S A       Date:  1995-09-12       Impact factor: 11.205

8.  Linkage analysis of familial Alzheimer disease, using chromosome 21 markers.

Authors:  G D Schellenberg; M A Pericak-Vance; E M Wijsman; D K Moore; P C Gaskell; L A Yamaoka; J L Bebout; L Anderson; K A Welsh; C M Clark
Journal:  Am J Hum Genet       Date:  1991-03       Impact factor: 11.025

9.  Presenilin-1 knockin mice reveal loss-of-function mechanism for familial Alzheimer's disease.

Authors:  Dan Xia; Hirotaka Watanabe; Bei Wu; Sang Hun Lee; Yan Li; Evgeny Tsvetkov; Vadim Y Bolshakov; Jie Shen; Raymond J Kelleher
Journal:  Neuron       Date:  2015-03-04       Impact factor: 17.173

Review 10.  Clinical genetics of Alzheimer's disease.

Authors:  Zhangyu Zou; Changyun Liu; Chunhui Che; Huapin Huang
Journal:  Biomed Res Int       Date:  2014-05-13       Impact factor: 3.411

  10 in total

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