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Sporadic Creutzfeldt-Jacob disease

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Sporadic CJD accounts for over 90% of cases of human prion disease.

The disease occurs worldwide with an annual incidence of one case per million population.

There are no known environmental risk factors.

Most patients with sporadic CJD are homozygous for methionine at the polymorphic position 129 in the prion protein.


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The content herein is provided for informational purposes and does not replace the need to apply professional clinical judgement when diagnosing or treating any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions.

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