Genetics of restless legs syndrome.

Abstract

Restless legs syndrome (RLS) is a common disorder, although under-diagnosed, with a prevalence of up to 15% depending on the population sampled. Familial aggregation has been widely shown since Ekbom formerly described the condition in 1960; twin studies support a genetic contribution in the development of this disorder. Molecular genetic approaches have identified three genomic regions in RLS susceptibility, however no specific mutations have yet been identified. Herein, we review the current status of genetics in RLS, providing some methodological guidelines to help future research.

Cite this paper

@article{Mata2006GeneticsOR, title={Genetics of restless legs syndrome.}, author={Ignacio Mata and Cynthia L. Bodkin and C H Adler and Siong-Chi Lin and Ryan J. Uitti and Matthew John Farrer and Zbigniew K Wszolek}, journal={Parkinsonism & related disorders}, year={2006}, volume={12 1}, pages={1-7} }