Two Chinese patients of sporadic Creutzfeldt–Jacob disease with a S97N mutation in PRNP gene

ABSTRACT

Worldwide, 10–15% human prion disease are genetic and inherited, due to the special mutations or insertions in PRNP gene. Herein, we reported two Chinese patients with rapidly progressive dementia who were referred to the national Creutzfeldt–Jacob disease (CJD) surveillance as suspected CJD. Those two patients displayed sporadic CJD (sCJD)-like clinical phenotype, e.g. rapidly progressive dementia, visional and mental problems, sCJD-associated abnormalities in MRI. A missense mutation was identified in one PRNP allele of these two patients, resulting in a change from serine to asparagine at codon 97 (S97N). RT-QuIC of the cerebrospinal fluid samples from those two cases were positive. It indicates that they are very likely to be prion disease.

KEYWORDS:

• CJD
• prion
• PRNP
• S97N mutation

Disclosure statement

No potential conflict of interest was reported by the author(s).

Additional information

Funding

This work was supported by Grant (2019SKLID501, 2019SKLID603, 2019SKLID307) from the State Key Laboratory for Infectious Disease Prevention and Control, China CDC.