Emerging parkinsonian phenotypes.

A E Elia, A Albanese

Journal: Revue neurologique 2010;166(10):834-40

PMID: 20817231

Abstract

There is no unique way to define Parkinson's disease (PD) clinically. "Classical parkinsonian features" can be found not only in sporadic idiopathic PD patients, but also in other parkinsonian disorders, such as genetic forms associated with mutations in PARK or in other genes. The present review will describe the parkinsonian phenotypes emerging from the new Mendelian genes which have been linked to PD (such as PARK9 and PARK14), the associated dystonia-parkinsonism disorders (such as the syndromes of neurodegeneration with brain iron accumulation) and the emerging data on heterozygous variants of genes which could influence the risk to develop PD and the PD phenotypes (like PD associated with glucose cerebrosidase mutations).

Copyright © 2010 Elsevier Masson SAS. All rights reserved.

Address: Fondazione, IRCCS Istituto Neurologico Carlo Besta, Università Cattolica del Sacro Cuore, Via G. Celoria 11, 20133 Milano, Italy.
Bant logo

© Copyright 2026, Nutrition Evidence

NED wishes to thank the following organisations for their support:

We use cookies to improve your experience and analyze site traffic with Google Analytics. By continuing to use our site, you agree to our use of cookies. Learn more.