| Literature DB >> 28278113 |
Qi Shi1, Kang Xiao1, Cao Chen1, Wei Zhou1, Chen Gao1, Jing Wang1, Bao-Yun Zhang1, Yuan Wang1, Xiao-Ping Dong1.
Abstract
Sporadic Creutzfeldt-Jakob disease (sCJD) occurs frequently in the relatively older population, mainly in the groups of 60-69 and 70-79 year-old. Since 2006 when China performed national CJD surveillance, 14 young probable sCJD patients below 40 year-old were identified, counting for 1.93% of all probable sCJD cases. The clinical features of young probable sCJD cases, including the onset feature, the presence of sCJD-associated signs and the clinical duration, are indistinguishable from those of older patients. Special sCJD-associated abnormalities on EEG and MRI were noticed in 7 and 10 cases. CSF 14-3-3 was positive in 7 cases. CSF RT-QuIC showed positive reactive curves in 9 cases, with short lag phases. PRNP sequencing did not find any mutation. Due to low rate of brain autopsy in China, performances of other CJD-associated examinations as much as possible are extremely important for the distinguish diagnosis of young probable sCJD patients.Entities:
Keywords: Creutzfeldt-Jakob disease; prion disease; sporadic; surveillance; young patient
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Year: 2017 PMID: 28278113 PMCID: PMC5399906 DOI: 10.1080/19336896.2017.1287656
Source DB: PubMed Journal: Prion ISSN: 1933-6896 Impact factor: 3.931