A retrospective study of Creutzfeldt-Jakob disease in Italy (1972–1986)
✍ Scribed by C. Masullo; M. Pocchiari; G. Neri; P. Casaccia; A. Iavarone; A. Ladogana; G. Macchi
- Publisher
- Springer
- Year
- 1988
- Tongue
- English
- Weight
- 482 KB
- Volume
- 4
- Category
- Article
- ISSN
- 0393-2990
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✦ Synopsis
In a retrospective study of Creutzfeldt-Jakob disease (CJD) in Italy from 1972 to 1986, we found 79 cases which fulfilled the diagnostic criteria for CJD. The annual mortality rate was 0.09 cases per million inhabitants. In this series the female to male ratio was 2.59, a value significantly higher than that found in Italian population (1.05). The mean age at death was 62.1 ___ 9.4 years and the mean duration of the disease was 5.3 + _ 3.0 months. No familial cases of CJD were found in our series. Mental deterioration was present in all of our cases, myoclonus in 85% and the other clinical signs were present at a lower rate. Periodic EEG activity was found in 92% of the cases. Two patients had had neurological or ophthalmic surgery and 17% of our cases had undergone general surgery within 5 years prior to the clinical onset of CJD.
📜 SIMILAR VOLUMES
We report a group of 13 cases of Creutzfeldt-Jakob disease treated in the region of Parma (Italy) between 1975 and 1984. An extensive study did not point to any common source of infection. The clinical stereotypy and distinctive neuropathology in this temporo-spatially confined group of patients mig
## Abstract A systematic search for cases of Creutzfeldt‐Jakob disease occurring in the ten‐year period 1968 through 1977 was conducted in the city of Paris and surrounding departments which comprise the greater Paris area. Fifty‐six cases were found among the total population of approximately 10 m