Creutzfeldt-Jakob disease (CJD) can also be diagnosed in a resource-limited setting through good clinical analysis. The diagnosis of CJD should be considered in patients with rapidly evolving neurological signs associated with cognitive disturbances even in countries with limited available sophisticated tools and where CJD was never reported before.
Keywords: Creutzfeldt‐Jakob disease; prion disorder; sporadic Creutzfeldt‐Jakob disease.
© 2019 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd.