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References OMIM Gene GeneReviews HGMD HGNC
last update : 21/05/2008
Symbol RLLS3
Location 9p24-p22
Name restless legs syndrome 3
Corresponding gene PTPRD
Main clinical features
  • acromelalgia hereditary, begining in adolescence, with myoclonic jerks occurred at night before sleep and severely interfered with it
  • diurnal occurrence of an urge to move, usually accompanied by uncomfortable sensations in the lower limbs
  • Genetic determination autosomal dominant
    Function/system disorder neurology
    Type susceptibility factor