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  • Mowat-Wilson syndrome Relevant markers:
    HypertelorismMegacolonShort corpus callosumSingle umbilical artery (SUA)Hydroureter
    Parents markers:
    HeartMicrocephalyVentricular septal defect (VSD)Pyelectasis/hydronephrosis
      Involved genes:
      (gene — definition — chromosome)      		ZEB2 — ZINC FINGER E BOX-BINDING HOMEOBOX 2 — 2q22.3
      Inheritance mode:AD
      Other online databases:OMIM
      References:
      2013 European Journal of Medical Genetics Case report Read on PubMed
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