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  • Prader-Willi syndrome Relevant markers:
    Asymmetric IUGR/SGABreech presentationClenched hand/sHypokinesiaPolyhydramniosSevere IUGR/SGA
    Parents markers:
    Intrauterine growth retardation (IUGR/SGA/FGR)
      Incidence:- — 1/100000
      Involved genes:
      (gene — definition — chromosome)      		NDN — NECDIN — 15q11.2, SNRPN — SMALL NUCLEAR RIBONUCLEOPROTEIN POLYPEPTIDE N — 15q11.2
      Inheritance mode:Sporadic (new mutation)
      Other online databases:OMIM
      References:
      2011 Genet Couns Read on PubMed
      2014 Am J Med Genet A Read on PubMed
      2015 J Obstet Gynaecol Case report Read on PubMed
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