Autosomal-Dominant Locus for Restless Legs Syndrome in French-Canadians on Chromosome 16p12.1

ArticleinMovement Disorders 24(1):40-50 · January 2009with9 Reads
Impact Factor: 5.68 · DOI: 10.1002/mds.22263 · Source: PubMed

    Abstract

    We describe an autosomal-dominant locus for Restless Legs Syndrome (RLS) in a French-Canadian (FC) pedigree. Genome-wide microsatellite scan and linkage analysis were used in this study. The locus maps to chromosome 16p12.1 and spans 1.18 Mega bases. The maximum multipoint LOD scores are of 3.5 over the total of 10 markers. Evidence for the same locus was also found in a smaller FC pedigree sime095. The analysis of the sequence of 8 annotated genes within the region did not reveal any pathogenic mutations. Copy number variation and karyotype analyses did not reveal any chromosomal abnormality in the region. Further analyses of the region are necessary to find the genetic cause of RLS in this family.