| Literature DB >> 11481705 |
Z K Wszolek1, R H Kardon, E C Wolters, R F Pfeiffer.
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. Copyright 2001 Movement Disorder Society.Entities:
Mesh:
Year: 2001 PMID: 11481705 DOI: 10.1002/mds.1131
Source DB: PubMed Journal: Mov Disord ISSN: 0885-3185 Impact factor: 10.338