Inherited prion disease (PrP lysine 200) in Britain: two case reports

Abstract

Objective: To identify cases of inherited prion diseases in Britain and to assess their phenotypic features.

Design: Screening study of patients suspected clinically to have Creutzfeldt-Jakob disease and other neurodegenerative diseases by prion protein gene analysis.

Setting: Biochemical research department.

Subjects: Patients suspected to have Creutzfeldt-Jakob disease and other neurodegenerative diseases.

Results: Two patients with symptoms characteristic of sporadic Creutzfeldt-Jakob disease were found to have inherited prion protein disease (PrP lysine 200), with a mutation at codon 200 of the prion protein gene. Both were homozygous at codon 129 of the gene. One patient was a man aged 58 of British descent while the other was of Libyan Jewish origin.

Conclusion: Two foci of inherited prion disease are known, among Libyan Jews and in Slovakia. A separate British focus of the disease may also exist. Heterozygosity at codon 129 may lead to reduced penetrance of the mutation.