Frontotemporal dementia and Parkinsonism linked to chromosome 17 (FTDP‐17): PPND family. A longitudinal videotape demonstration
Identifieur interne : 004797 ( Main/Exploration ); précédent : 004796; suivant : 004798Frontotemporal dementia and Parkinsonism linked to chromosome 17 (FTDP‐17): PPND family. A longitudinal videotape demonstration
Auteurs : Zbigniew K. Wszolek [États-Unis] ; Randy H. Kardon [États-Unis] ; Erik Ch. Wolters [Pays-Bas] ; Ronald F. Pfeiffer [États-Unis]Source :
- Movement Disorders [ 0885-3185 ] ; 2001-07.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Homme.
English descriptors
- KwdEn :
- Adult, Chromosome E17, Chromosomes, Human, Pair 17, Dementia, Dementia (diagnosis), Dementia (genetics), Evolution, Family study, Follow-Up Studies, Frontal lobe, Genetic Linkage (genetics), Human, Humans, Male, Middle Aged, Neurologic Examination, Parkinson disease, Parkinsonian Disorders (diagnosis), Parkinsonian Disorders (genetics), Temporal lobe, Video recording, Videotape Recording.
- MESH :
- diagnosis : Dementia, Parkinsonian Disorders.
- genetics : Dementia, Genetic Linkage, Parkinsonian Disorders.
- Adult, Chromosomes, Human, Pair 17, Follow-Up Studies, Humans, Male, Middle Aged, Neurologic Examination, Videotape Recording.
Abstract
Frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP‐17), characterized by an autosomal dominant inheritance pattern, has recently been recognized as a distinct entity that can display a confusingly broad clinical phenotype. The pallido‐ponto‐nigral degeneration (PPND) variant is the prototypical example of the parkinsonism‐predominant pattern of FTDP‐17. A longitudinal videotape demonstration of the clinical progression of this entity in a single individual, along with brief videotape segments from three additional affected individuals, is presented in order to facilitate recognition of this disorder. © 2001 Movement Disorder Society.
Url:
DOI: 10.1002/mds.1131
Affiliations:
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Le document en format XML
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<idno type="eISSN">1531-8257</idno>
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<term>Dementia (diagnosis)</term>
<term>Dementia (genetics)</term>
<term>Evolution</term>
<term>Family study</term>
<term>Follow-Up Studies</term>
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<term>Genetic Linkage (genetics)</term>
<term>Human</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Neurologic Examination</term>
<term>Parkinson disease</term>
<term>Parkinsonian Disorders (diagnosis)</term>
<term>Parkinsonian Disorders (genetics)</term>
<term>Temporal lobe</term>
<term>Video recording</term>
<term>Videotape Recording</term>
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<term>Parkinsonian Disorders</term>
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<term>Parkinsonian Disorders</term>
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<term>Follow-Up Studies</term>
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<term>Male</term>
<term>Middle Aged</term>
<term>Neurologic Examination</term>
<term>Videotape Recording</term>
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<term>Evolution</term>
<term>Homme</term>
<term>Lobe frontal</term>
<term>Lobe temporal</term>
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<front><div type="abstract" xml:lang="en">Frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP‐17), characterized by an autosomal dominant inheritance pattern, has recently been recognized as a distinct entity that can display a confusingly broad clinical phenotype. The pallido‐ponto‐nigral degeneration (PPND) variant is the prototypical example of the parkinsonism‐predominant pattern of FTDP‐17. A longitudinal videotape demonstration of the clinical progression of this entity in a single individual, along with brief videotape segments from three additional affected individuals, is presented in order to facilitate recognition of this disorder. © 2001 Movement Disorder Society.</div>
</front>
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<name sortKey="Kardon, Randy H" sort="Kardon, Randy H" uniqKey="Kardon R" first="Randy H." last="Kardon">Randy H. Kardon</name>
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<country name="Pays-Bas"><region name="Hollande-Septentrionale"><name sortKey="Wolters, Erik Ch" sort="Wolters, Erik Ch" uniqKey="Wolters E" first="Erik Ch." last="Wolters">Erik Ch. Wolters</name>
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