Document Detail


Frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17): PPND family. A longitudinal videotape demonstration.
MedLine Citation:
PMID:  11481705     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
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.
Authors:
Z K Wszolek; R H Kardon; E C Wolters; R F Pfeiffer
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Publication Detail:
Type:  Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  Movement disorders : official journal of the Movement Disorder Society     Volume:  16     ISSN:  0885-3185     ISO Abbreviation:  Mov. Disord.     Publication Date:  2001 Jul 
Date Detail:
Created Date:  2001-08-01     Completed Date:  2001-10-18     Revised Date:  2007-11-14    
Medline Journal Info:
Nlm Unique ID:  8610688     Medline TA:  Mov Disord     Country:  United States    
Other Details:
Languages:  eng     Pagination:  756-60     Citation Subset:  IM    
Copyright Information:
Copyright 2001 Movement Disorder Society.
Affiliation:
Department of Neurology, Mayo Clinic, Jacksonville, Florida, USA.
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MeSH Terms
Descriptor/Qualifier:
Adult
Chromosomes, Human, Pair 17*
Dementia / diagnosis,  genetics*
Follow-Up Studies
Humans
Linkage (Genetics) / genetics*
Male
Middle Aged
Neurologic Examination
Parkinsonian Disorders / diagnosis,  genetics*
Videotape Recording
Grant Support
ID/Acronym/Agency:
5Z5960//PHS HHS; NS40256-01C2J/NS/NINDS NIH HHS; P01AG17216/AG/NIA NIH HHS

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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