Coexistence of movement disorders and epilepsia partialis continua as the initial signs in probable Creutzfeldt-Jakob disease.
Identifieur interne : 003184 ( PubMed/Checkpoint ); précédent : 003183; suivant : 003185Coexistence of movement disorders and epilepsia partialis continua as the initial signs in probable Creutzfeldt-Jakob disease.
Auteurs : Berril Donmez [Turquie] ; Raif Cakmur ; Süleyman Men ; Ibrahim Oztura ; Arzu KitisSource :
- Movement disorders : official journal of the Movement Disorder Society [ 0885-3185 ] ; 2005.
English descriptors
- KwdEn :
- Basal Ganglia (pathology), Caudate Nucleus (physiopathology), Creutzfeldt-Jakob Syndrome (epidemiology), Creutzfeldt-Jakob Syndrome (pathology), Diagnosis, Differential, Electroencephalography, Epilepsies, Partial (diagnosis), Epilepsies, Partial (epidemiology), Epilepsies, Partial (physiopathology), Female, Gyrus Cinguli (physiopathology), Humans, Magnetic Resonance Imaging, Middle Aged, Movement Disorders (diagnosis), Movement Disorders (epidemiology), Movement Disorders (physiopathology), Putamen (physiopathology), Severity of Illness Index, Thalamus (physiopathology).
- MESH :
- diagnosis : Epilepsies, Partial, Movement Disorders.
- epidemiology : Creutzfeldt-Jakob Syndrome, Epilepsies, Partial, Movement Disorders.
- pathology : Basal Ganglia, Creutzfeldt-Jakob Syndrome.
- physiopathology : Caudate Nucleus, Epilepsies, Partial, Gyrus Cinguli, Movement Disorders, Putamen, Thalamus.
- Diagnosis, Differential, Electroencephalography, Female, Humans, Magnetic Resonance Imaging, Middle Aged, Severity of Illness Index.
Abstract
Movement disorders and epilepsy rarely occur in the early stage of Creutzfeldt-Jakob disease (CJD) but have not been reported concurrently. We report on a 47-year-old patient with probable CJD who presented with generalized chorea and focal dystonia with myoclonic jerks on the right hand. Myoclonic jerks progressed to epilepsia partialis continua within 5 days of admission to the hospital. The diagnosis of our patient was compatible with probable CJD on the basis of clinical course, electroencephalogram, and diffusion-weighted magnetic resonance imaging findings, and presence of 14-3-3 protein in cerebrospinal fluid. To our knowledge, this is the first report of a case developing both movement disorders and epilepsia partialis continua in the early stage of the disease.
DOI: 10.1002/mds.20502
PubMed: 15895425
Affiliations:
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We report on a 47-year-old patient with probable CJD who presented with generalized chorea and focal dystonia with myoclonic jerks on the right hand. Myoclonic jerks progressed to epilepsia partialis continua within 5 days of admission to the hospital. The diagnosis of our patient was compatible with probable CJD on the basis of clinical course, electroencephalogram, and diffusion-weighted magnetic resonance imaging findings, and presence of 14-3-3 protein in cerebrospinal fluid. To our knowledge, this is the first report of a case developing both movement disorders and epilepsia partialis continua in the early stage of the disease.</div></front></TEI><pubmed><MedlineCitation Owner="NLM" Status="MEDLINE"><PMID Version="1">15895425</PMID><DateCreated><Year>2005</Year><Month>08</Month><Day>29</Day></DateCreated><DateCompleted><Year>2005</Year><Month>12</Month><Day>20</Day></DateCompleted><Article PubModel="Print"><Journal><ISSN IssnType="Print">0885-3185</ISSN><JournalIssue CitedMedium="Print"><Volume>20</Volume><Issue>9</Issue><PubDate><Year>2005</Year><Month>Sep</Month></PubDate></JournalIssue><Title>Movement disorders : official journal of the Movement Disorder Society</Title><ISOAbbreviation>Mov. Disord.</ISOAbbreviation></Journal><ArticleTitle>Coexistence of movement disorders and epilepsia partialis continua as the initial signs in probable Creutzfeldt-Jakob disease.</ArticleTitle><Pagination><MedlinePgn>1220-3</MedlinePgn></Pagination><Abstract><AbstractText>Movement disorders and epilepsy rarely occur in the early stage of Creutzfeldt-Jakob disease (CJD) but have not been reported concurrently. We report on a 47-year-old patient with probable CJD who presented with generalized chorea and focal dystonia with myoclonic jerks on the right hand. Myoclonic jerks progressed to epilepsia partialis continua within 5 days of admission to the hospital. The diagnosis of our patient was compatible with probable CJD on the basis of clinical course, electroencephalogram, and diffusion-weighted magnetic resonance imaging findings, and presence of 14-3-3 protein in cerebrospinal fluid. 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ValidYN="Y"><LastName>Kitis</LastName><ForeName>Arzu</ForeName><Initials>A</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D002363">Case Reports</PublicationType><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>Mov Disord</MedlineTA><NlmUniqueID>8610688</NlmUniqueID><ISSNLinking>0885-3185</ISSNLinking></MedlineJournalInfo><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName MajorTopicYN="N" UI="D001479">Basal Ganglia</DescriptorName><QualifierName MajorTopicYN="N" UI="Q000473">pathology</QualifierName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D002421">Caudate Nucleus</DescriptorName><QualifierName MajorTopicYN="N" UI="Q000503">physiopathology</QualifierName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D007562">Creutzfeldt-Jakob 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Index</DescriptorName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D013788">Thalamus</DescriptorName><QualifierName MajorTopicYN="N" UI="Q000503">physiopathology</QualifierName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>2005</Year><Month>5</Month><Day>17</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2005</Year><Month>12</Month><Day>21</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2005</Year><Month>5</Month><Day>17</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="doi">10.1002/mds.20502</ArticleId><ArticleId IdType="pubmed">15895425</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list><country><li>Turquie</li></country></list><tree><noCountry><name sortKey="Cakmur, Raif" sort="Cakmur, Raif" uniqKey="Cakmur R" first="Raif" last="Cakmur">Raif Cakmur</name><name sortKey="Kitis, Arzu" sort="Kitis, Arzu" uniqKey="Kitis A" first="Arzu" last="Kitis">Arzu Kitis</name><name sortKey="Men, Suleyman" sort="Men, Suleyman" uniqKey="Men S" first="Süleyman" last="Men">Süleyman Men</name><name sortKey="Oztura, Ibrahim" sort="Oztura, Ibrahim" uniqKey="Oztura I" first="Ibrahim" last="Oztura">Ibrahim Oztura</name></noCountry><country name="Turquie"><noRegion><name sortKey="Donmez, Berril" sort="Donmez, Berril" uniqKey="Donmez B" first="Berril" last="Donmez">Berril Donmez</name></noRegion></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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