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About: Emanuel syndrome     Goto   Sponge   NotDistinct   Permalink

An Entity of Type : yago:Trisomy114504558, within Data Space : dbpedia.demo.openlinksw.com associated with source document(s)

Type: ThingDiseaseyago:WikicatAutosomalTrisomiesyago:WikicatChromosomalAbnormalitiesyago:Aberrance114503665yago:Abnormality114501726yago:Abstraction100002137yago:Attribute100024264yago:ChromosomalAberration114504103yago:Condition113920835yago:Disease114070360yago:GeneticDisease114151139yago:IllHealth114052046yago:Illness114061805yago:PathologicalState114051917yago:PhysicalCondition114034177yago:WikicatGeneticDisordersdiseaseyago:State100024720yago:Trisomy114504558 New Facet based on Instances of this Class

Emanuel syndrome, also known as derivative 22 syndrome, or der(22) syndrome, is a rare disorder associated with multiple congenital anomalies, including profound intellectual disability, preauricular skin tags or pits, and conotruncal heart defects. It can occur in offspring of carriers of the constitutional chromosomal translocation t(11;22)(q23;q11), owing to a 3:1 meiotic malsegregation event resulting in partial trisomy of chromosomes 11 and 22. An unbalanced translocation between chromosomes 11 and 22 is described as Emanuel syndrome. It was first described in 1980 by American medical researchers Beverly S. Emanuel and Elaine H. Zackai, and a consortium of European scientists the same year.