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  • 15q25-q26 deletion syndrome Relevant markers:
    Congenital diaphragmatic hernia (CDH)TalipesNuchal edema/fold/Increased nuchal translucency (NT)/cystic hygromaCerebellar hypoplasiaOverriding aortaBroad nasal bridgeFlat noseHypertelorismDouble outlet right ventricle (DORV)Atrial septal defect (ASD)Hypoplastic aorta
    Parents markers:
    Intrauterine growth retardation (IUGR/SGA/FGR)Ventricular septal defect (VSD)Atrioventricular septal defect (AVSD)
      Involved genes:
      (gene — definition — chromosome)      		15q25
      Inheritance mode:AD
      Other online databases:OMIM
      References:
      2001 Prenat Diagn Case report Read on PubMed
      2007 Am J Med Genet A Case report Read on PubMed
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