Frontotemporal dementia and Parkinsonism linked to chromosome 17 (FTDP‐17): PPND family. A longitudinal videotape demonstration
Identifieur interne : 006C79 ( Main/Merge ); précédent : 006C78; suivant : 006C80Frontotemporal 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.
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.
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DOI: 10.1002/mds.1131
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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>
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