Literature DB >> 19571725

A case of dementia with PRNP D178Ncis-129M and no insomnia.

Rita J Guerreiro1, Tina Vaskov, Cynthia Crews, Andrew Singleton, John Hardy.   

Abstract

OBJECTIVE: To describe a dementia case clinically diagnosed as Alzheimer disease with a PRNP genotype usually associated with familial fatal insomnia.
METHODS: Polymerase chain reaction amplification and subsequent direct sequencing of PGRN, MAPT, PSEN1, PSEN2, APP, and PRNP genes.
RESULTS: A point mutation (D178N) was found in the PRNP gene.
CONCLUSIONS: The mutation D178N in the PRNP gene associated with the M129 genotype is usually associated with familial fatal insomnia. However, a few cases have been reported with different clinical phenotypes. Here, we describe one of these cases and stress the importance of genetic screening of PRNP in early onset dementia cases.

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Year:  2009        PMID: 19571725      PMCID: PMC2787867          DOI: 10.1097/WAD.0b013e3181ae3a76

Source DB:  PubMed          Journal:  Alzheimer Dis Assoc Disord        ISSN: 0893-0341            Impact factor:   2.703


  24 in total

1.  Familial Creutzfeldt-Jakob disease with D178N-129M mutation of PRNP presenting as cerebellar ataxia without insomnia.

Authors:  Y Taniwaki; H Hara; K Doh-Ura; I Murakami; H Tashiro; T Yamasaki; H Shigeto; K Arakawa; E Araki; T Yamada; T Iwaki; J Kira
Journal:  J Neurol Neurosurg Psychiatry       Date:  2000-03       Impact factor: 10.154

2.  The D178N (cis-129M) "fatal familial insomnia" mutation associated with diverse clinicopathologic phenotypes in an Australian kindred.

Authors:  C A McLean; E Storey; R J Gardner; A E Tannenberg; L Cervenáková; P Brown
Journal:  Neurology       Date:  1997-08       Impact factor: 9.910

Review 3.  Prion diseases.

Authors:  R S G Knight; R G Will
Journal:  J Neurol Neurosurg Psychiatry       Date:  2004-03       Impact factor: 10.154

4.  High prevalence of pathogenic mutations in patients with early-onset dementia detected by sequence analyses of four different genes.

Authors:  U Finckh; T Müller-Thomsen; U Mann; C Eggers; J Marksteiner; W Meins; G Binetti; A Alberici; C Hock; R M Nitsch; A Gal
Journal:  Am J Hum Genet       Date:  2000-01       Impact factor: 11.025

Review 5.  New frontiers in Alzheimer's disease genetics.

Authors:  R E Tanzi; L Bertram
Journal:  Neuron       Date:  2001-10-25       Impact factor: 17.173

6.  Phenotypic characteristics of familial Creutzfeldt-Jakob disease associated with the codon 178Asn PRNP mutation.

Authors:  P Brown; L G Goldfarb; J Kovanen; M Haltia; F Cathala; M Sulima; C J Gibbs; D C Gajdusek
Journal:  Ann Neurol       Date:  1992-03       Impact factor: 10.422

7.  Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease.

Authors:  G McKhann; D Drachman; M Folstein; R Katzman; D Price; E M Stadlan
Journal:  Neurology       Date:  1984-07       Impact factor: 9.910

8.  Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: the phenotype of the stop codon 145 mutation in PRNP.

Authors:  B Ghetti; P Piccardo; M G Spillantini; Y Ichimiya; M Porro; F Perini; T Kitamoto; J Tateishi; C Seiler; B Frangione; O Bugiani; G Giaccone; F Prelli; M Goedert; S R Dlouhy; F Tagliavini
Journal:  Proc Natl Acad Sci U S A       Date:  1996-01-23       Impact factor: 11.205

9.  Heterogeneity in dementia of the Alzheimer type: evidence of subgroups.

Authors:  R Mayeux; Y Stern; S Spanton
Journal:  Neurology       Date:  1985-04       Impact factor: 9.910

10.  Ultrastructural study of florid plaques in variant Creutzfeldt-Jakob disease: a comparison with amyloid plaques in kuru, sporadic Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker disease.

Authors:  B Sikorska; P P Liberski; T Sobów; H Budka; J W Ironside
Journal:  Neuropathol Appl Neurobiol       Date:  2008-05-30       Impact factor: 8.090

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  4 in total

Review 1.  Genetic PrP Prion Diseases.

Authors:  Mee-Ohk Kim; Leonel T Takada; Katherine Wong; Sven A Forner; Michael D Geschwind
Journal:  Cold Spring Harb Perspect Biol       Date:  2018-05-01       Impact factor: 10.005

2.  Familial fatal insomnia with atypical clinical features in a patient with D178N mutation and homozygosity for Met at codon 129 of the prion protein gene.

Authors:  Lin Sun; Xia Li; Xiang Lin; Feng Yan; Kathryn Chen; Shifu Xiao
Journal:  Prion       Date:  2015       Impact factor: 3.931

Review 3.  Genetic prion disease: Experience of a rapidly progressive dementia center in the United States and a review of the literature.

Authors:  Leonel T Takada; Mee-Ohk Kim; Ross W Cleveland; Katherine Wong; Sven A Forner; Ignacio Illán Gala; Jamie C Fong; Michael D Geschwind
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2017-01       Impact factor: 3.568

4.  Mutational analysis of PRNP in Alzheimer's disease and frontotemporal dementia in China.

Authors:  Weiwei Zhang; Bin Jiao; Tingting Xiao; Chuzheng Pan; Xixi Liu; Lin Zhou; Beisha Tang; Lu Shen
Journal:  Sci Rep       Date:  2016-12-02       Impact factor: 4.379

  4 in total

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