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Genetics of restless legs syndrome (RLS): State-of-the-art and future directions
ISSN
0885-3185
Date Issued
2007
Author(s)
Winkelmann, Juliane
Polo, Oli
Provini, Federica
Nevsimalova, Sonja
Kemlink, David
Sonka, Karel
Hoegl, Birgit
Poewe, Werner
Stiasny-Kolster, Karin
Oertel, Wolfgang
de Weerd, A. L.
Strambi, Luigi Ferini
Zucconi, Marco
Pramstaller, Peter P.
Arnulf, Isabelle
Klein, Christine
Hadjigeorgiou, Georgios M.
Rye, David
Montagna, Pasquale
DOI
10.1002/mds.21587
Abstract
Several studies demonstrated that 60% of restless legs syndrome (RLS) patients have a positive family history and it has been suggested that RLS is a highly hereditary trait. To date, several loci have been mapped but no gene has been identified yet. Phenocopies and possible nonpenetrants made it difficult to detect a common segregating haplotype within the families. Defining the exact candidate region is hampered by possible intrafamilial, allelic, and nonallelic heterogeneity. One important prerequisite for future successful genetic studies in RLS is the availability of large and thoroughly phenotyped patients and family samples for linkage as well as association studies. (C) 2007 Movement Disorder Society.