Progressive myoclonic cerebellar ataxia as a manifestation of Creutzfeldt-Jakob disease

Progressive myoclonic cerebellar ataxia is a clinical entity with an important spectrum of possible diagnoses that requires a complex and exhaustive differential diagnosis. A 53-year-old male patient with no relevant medical history who was admitted to hospital because of an unstable gait, together...

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Bibliographic Details

Published in:	Revista de neurologiá Vol. 37; no. 6; pp. 535 - 538
Main Authors:	Santos, S, Pascual-Millán, L F, Escalza-Codina, I, Navas-Vinagre, I, López del Val, L J, Mostacero-Miguel, E, Ramón y Cajal, S
Format:	Journal Article
Language:	Spanish
Published:	Spain 16-09-2003
Subjects:	Cerebellar Ataxia - etiology Cerebellar Ataxia - pathology Creutzfeldt-Jakob Syndrome - complications Creutzfeldt-Jakob Syndrome - diagnosis Creutzfeldt-Jakob Syndrome - pathology Fatal Outcome Humans Male Middle Aged Myoclonus - etiology Myoclonus - pathology
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