A three-sister sibship of Gerstmann-Straussler-Scheinker disease with a CJD phenotype

K. Majtényi, P. Brown, L. Cervenáková, L. G. Goldfarb, J. Tateishi

Research output: Contribution to journalArticle

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Abstract

Objective: To describe a rare phenotypic variant of P102L Gerstmann- Straussler-Scheinker disease (GSS). Background: Classic GSS is characterized by an early age at onset, prominent cerebellar signs with a slowly evolving dementia, and a neuropathology including multifocal PrP-positive plaques and variable but usually modest spongiform change. Methods: Clinical, neuropathologic, immunohistochemical, and molecular genetic analysis of three sisters in a Hungarian family was performed. Results: The clinical course of all three sisters was indistinguishable from sporadic Creutzfeldt-Jakob disease (CJD). Neuropathologic examination revealed spongiform changes, PrP (prion)-positive unicentric 'kuru' or multicentric plaques, and abundant β- A4-positive senile plaques. Molecular genetic analysis of the PRNP gene showed the heterozygous codon P102L mutation of classic GSS, with the methionine encoding allele of a heterozygous codon 129 coupled to the mutant 102 allele. Conclusion: The authors report the second recorded example of a sporadic CJD phenotype occurring in association with the P102L GSS genotype, and the first instance in which the phenotype was the rule rather than the exception, or was associated with prominent β-A4 plaque formation.

Original languageEnglish
Pages (from-to)2133-2137
Number of pages5
JournalNeurology
Volume54
Issue number11
Publication statusPublished - Jun 13 2000

Fingerprint

Gerstmann-Straussler-Scheinker Disease
Creutzfeldt-Jakob Syndrome
Phenotype
Codon
Molecular Biology
Kuru
Alleles
Prions
Amyloid Plaques
Age of Onset
Methionine
Dementia
Genotype
Mutation
Genes

Keywords

  • Creutzfeldt-Jakob disease
  • Gerstmann-Straussler-Scheinker disease
  • Phenotype

ASJC Scopus subject areas

  • Neuroscience(all)

Cite this

Majtényi, K., Brown, P., Cervenáková, L., Goldfarb, L. G., & Tateishi, J. (2000). A three-sister sibship of Gerstmann-Straussler-Scheinker disease with a CJD phenotype. Neurology, 54(11), 2133-2137.

A three-sister sibship of Gerstmann-Straussler-Scheinker disease with a CJD phenotype. / Majtényi, K.; Brown, P.; Cervenáková, L.; Goldfarb, L. G.; Tateishi, J.

In: Neurology, Vol. 54, No. 11, 13.06.2000, p. 2133-2137.

Research output: Contribution to journalArticle

Majtényi, K, Brown, P, Cervenáková, L, Goldfarb, LG & Tateishi, J 2000, 'A three-sister sibship of Gerstmann-Straussler-Scheinker disease with a CJD phenotype', Neurology, vol. 54, no. 11, pp. 2133-2137.
Majtényi K, Brown P, Cervenáková L, Goldfarb LG, Tateishi J. A three-sister sibship of Gerstmann-Straussler-Scheinker disease with a CJD phenotype. Neurology. 2000 Jun 13;54(11):2133-2137.
Majtényi, K. ; Brown, P. ; Cervenáková, L. ; Goldfarb, L. G. ; Tateishi, J. / A three-sister sibship of Gerstmann-Straussler-Scheinker disease with a CJD phenotype. In: Neurology. 2000 ; Vol. 54, No. 11. pp. 2133-2137.
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