Frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17): PPND family. A longitudinal videotape demonstration

Zbigniew K Wszolek, Randy H. Kardon, Erik Ch Wolters, Ronald F. Pfeiffer

Research output: Contribution to journalArticle

8 Citations (Scopus)

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.

Original languageEnglish (US)
Pages (from-to)756-760
Number of pages5
JournalMovement Disorders
Volume16
Issue number4
DOIs
StatePublished - Jul 2001

Fingerprint

Frontotemporal Dementia
Chromosomes, Human, Pair 17
Videotape Recording
Parkinsonian Disorders
Substantia Nigra
Inheritance Patterns
Phenotype

ASJC Scopus subject areas

  • Clinical Neurology
  • Neuroscience(all)

Cite this

Frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17) : PPND family. A longitudinal videotape demonstration. / Wszolek, Zbigniew K; Kardon, Randy H.; Wolters, Erik Ch; Pfeiffer, Ronald F.

In: Movement Disorders, Vol. 16, No. 4, 07.2001, p. 756-760.

Research output: Contribution to journalArticle

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