Klug Genevieve M, Boyd Alison, Lewis Victoria, Kvasnicka Madga, Lee James S, Masters Colin L, Collins Steven J
Department of Pathology, The University of Melbourne, Victoria.
Commun Dis Intell Q Rep. 2005;29(3):269-71. doi: 10.33321/cdi.2005.29.25.
The Australian National Creutzfeldt-Jakob Disease Registry (ANCJDR) was established in October 1993 after the identification of probable iatrogenic CJD in recipients of human pituitary hormones. Since this time and with the recommendations of the Allars inquiry into CJD in Australia, the registry has performed surveillance of CJD in Australia with retrospective ascertainment to 1970 and ongoing prospective ascertainment of all human prion diseases or transmissible spongiform encephalopathies (TSEs). Prion diseases include CJD, Gerstmann-Straussler-Scheinker syndrome, fatal familial insomnia and Kuru. This brief summary presents the epidemiological findings of the ANCJDR based on data from 1970 to 31 December, 2004.
澳大利亚克雅氏病国家登记处（ANCJDR）于1993年10月在确诊接受人类垂体激素治疗的患者可能患有医源性克雅氏病后成立。自那时起，根据阿拉尔斯对澳大利亚克雅氏病的调查建议，该登记处对澳大利亚的克雅氏病进行了监测，追溯至1970年，并对所有人类朊病毒病或传染性海绵状脑病（TSE）进行持续的前瞻性确诊。朊病毒病包括克雅氏病、格斯特曼-施特劳斯勒-谢inker综合征、致死性家族性失眠症和库鲁病。本简要概述基于1970年至2004年12月31日的数据呈现了ANCJDR的流行病学调查结果。
