Erschienen in:
01.07.2020 | Letter to the Editor
Diagnosis of severe cognitive disorder: the family history as a key issue
verfasst von:
Céline Derollez, MD, Stéphane Haik, Florence Pasquier, MD PhD, Bertrand De Toffol, MD PhD, Stéphanie Bombois, MD
Erschienen in:
Neurological Sciences
|
Ausgabe 7/2020
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Excerpt
Familial Creutzfeldt-Jakob disease (fCJD) is a genetic prion disease and a rare condition presenting with varied clinical features making its diagnosis challenging due to overlaps with other rapid progressive dementias (RPD). Paraclinical tests remained essential to avoid incorrect diagnosis. Nevertheless, family history may be the key to a genetic diagnosis process. We reported the case of a patient investigated in the Department of Neurology at the University Hospital of Lille, France. …