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Frontotemporal dementia and parkinsonism linked to chromosome 17

Frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17) is an autosomal dominant neurodegenerative disorder and Parkinson plus syndrome,[1] which has three cardinal features: behavioral and personality changes, cognitive impairment, and motor symptoms. FTDP-17 was defined during the International Consensus Conference in Ann Arbor, Michigan, in 1996.

Frontotemporal dementia and parkinsonism linked to chromosome 17
Autosomal dominant - en.svg
This condition is inherited in an autosomal dominant manner.
SpecialtyNeurology Edit this on Wikidata

Contents

PathophysiologyEdit

The pathogenetic mechanisms underlying the disorder are thought to be related to the altered proportion of tau isoforms or to the ability of tau to bind microtubules and to promote microtubule assembly.

DiagnosisEdit

Definitive diagnosis of FTDP-17 requires a combination of characteristic clinical and pathological features and molecular genetic analysis. Genetic counseling should be offered to affected and at-risk individuals; for most subtypes, penetrance is incomplete.

ManagementEdit

Currently, treatment for FTDP-17 is only symptomatic and supportive.

PrognosisEdit

The prognosis and rate of the diseases progression vary considerably among individual patients and genetic kindreds, ranging from life expectancies of several months to several years, and, in exceptional cases, as long as two decades.

EpidemiologyEdit

The prevalence and incidence remain unknown but FTDP-17 is an extremely rare condition. It is caused by mutations in the MAPT gene, which encodes a microtubule-binding protein. Over 100 families with 38 different mutations in the tau gene have been identified worldwide. The phenotype of FTDP-17 varies not only between families carrying different mutations but also between and within families carrying the same mutations.

ReferencesEdit

  1. ^ Mitra K, Gangopadhaya PK, Das SK. (Jun 2003). "Parkinsonism plus syndrome--a review". Neurology India. 51 (2): 183–8. PMID 14570999.CS1 maint: Uses authors parameter (link)

Further readingEdit

  • Zbigniew K Wszolek, Yoshio Tsuboi, Bernardino Ghetti, Stuart Pickering-Brown, Yasuhiko Baba and William P Cheshire Orphanet Journal of Rare Diseases 2006, 1:30 doi:10.1186/1750-1172-1-30

External linksEdit

Classification