Focal dystonia as the presenting sign in Creutzfeldt‐Jakob disease
Identifieur interne : 004458 ( Main/Curation ); précédent : 004457; suivant : 004459Focal dystonia as the presenting sign in Creutzfeldt‐Jakob disease
Auteurs : Mark A. Hellmann [Israël] ; Eldad Melamed [Israël]Source :
- Movement Disorders [ 0885-3185 ] ; 2002-09.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Homme.
English descriptors
- KwdEn :
- Case study, Codon, Creutzfeldt Jakob disease, Creutzfeldt-Jakob Syndrome (complications), Creutzfeldt-Jakob Syndrome (diagnosis), Creutzfeldt-Jakob Syndrome (genetics), DNA Mutational Analysis, Diagnosis, Differential, Dystonia, Dystonic Disorders (diagnosis), Dystonic Disorders (etiology), Female, Focal lesion, Frontal Lobe (pathology), Human, Humans, Inaugural sign, Magnetic Resonance Imaging, Middle Aged, Point Mutation (genetics), Prion, Severity of Illness Index.
- MESH :
- chemical : Codon.
- complications : Creutzfeldt-Jakob Syndrome.
- diagnosis : Creutzfeldt-Jakob Syndrome, Dystonic Disorders.
- etiology : Dystonic Disorders.
- genetics : Creutzfeldt-Jakob Syndrome, Point Mutation.
- pathology : Frontal Lobe.
- DNA Mutational Analysis, Diagnosis, Differential, Female, Humans, Magnetic Resonance Imaging, Middle Aged, Severity of Illness Index.
Abstract
A variety of movement disorders may occur during the course of prion disease. We describe a unique patient who had focal upper limb dystonia as the presenting symptom of familial codon 200 mutation‐positive Creutzfeldt‐Jakob disease. © 2002 Movement Disorder Society
Url:
DOI: 10.1002/mds.10232
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<front><div type="abstract" xml:lang="en">A variety of movement disorders may occur during the course of prion disease. We describe a unique patient who had focal upper limb dystonia as the presenting symptom of familial codon 200 mutation‐positive Creutzfeldt‐Jakob disease. © 2002 Movement Disorder Society</div>
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