Restless Legs Syndrome, Susceptibility To, 1; Rls1

Description

Restless legs syndrome (RLS) is a neurologic sleep/wake disorder characterized by uncomfortable and unpleasant sensations in the legs that appear at rest, usually at night, inducing an irresistible desire to move the legs. The disorder results in nocturnal insomnia and chronic sleep deprivation (Bonati et al., 2003). Genetic Heterogeneity of Restless Legs SyndromeRLS1 has been mapped to chromosome 12q. Other susceptibility loci for RLS include RLS2 (OMIM ) on chromosome 14q13-q31; RLS3 (OMIM ) on chromosome 9p24-p22; RLS4 (OMIM ) on chromosome 2q33; RLS5 (OMIM ) on chromosome 20p13; RLS6 (OMIM ) on chromosome 6p21; RLS7 (OMIM ) on chromosome 2p14; and RLS8 (OMIM ) on chromosome 5q31.

Clinical Features

Top most frequent phenotypes and symptoms related to Restless Legs Syndrome, Susceptibility To, 1; Rls1

  • Anemia
  • Myoclonus
  • Hyperactivity
  • Attention deficit hyperactivity disorder
  • Pruritus
  • Abnormality of movement
  • Paresthesia
  • Sleep disturbance
  • Involuntary movements
  • Stereotypy

And another 8 symptoms. If you need more information about this disease we can help you.

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Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
No data available about the known clinical features onset.

Alternative names

Restless Legs Syndrome, Susceptibility To, 1; Rls1 Is also known as ekbom syndrome, acromelalgia, hereditary.

Researches and researchers

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Sources and references

You can check the following sources for additional information.

OMIM MESH Rare Disease Symptoms Checker

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