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Heredity of restless legs syndrome in a pregnant population
Objective:
To synthesize published research on genetic and heredity findings related to restless legs syndrome (RLS) in a pregnant population.
Data Sources:
PubMed, CINAHL, and PsycINFO databases and reference lists from published articles.
Study Selection:
Literature searches were conducted for primary research studies published in English on the genetic and heredity findings of RLS in pregnant populations.
Data Extraction:
Study characteristics and findings related to genetic and heredity aspects of RLS in a pregnant population.
Data Synthesis:
Five data-based articles met the criteria for study inclusion. Study findings comprised Level-2 and Level-3 evidence. Four of the five studies were larger population studies and contained a subset of pregnant participants. Parity and family history were important predictors of RLS proband status. Probands reported symptoms were often initiated during or after pregnancy.
Conclusions:
Symptoms of RLS for female probands are often initiated during pregnancy or after childbirth. A history of RLS in a previous pregnancy and family history of RLS were strong predictors of RLS in the current pregnancy. Future research on genetic associations of RLS in pregnancy is warranted.
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