Setleis lpar;bitemporal 'forceps marks'rpar; syndrome in a German familyevidence for autosomal dominant inheritance

摘要

The Setleis syndrome is a rare disorder characterized by predominantly facial findings, including bitemporal skin changes resembling forceps marks. Autosomal recessive inheritance of this distinct condition has been proposed. We report on a typically affected German boy whose father shows a much milder expression, thus suggesting autosomal dominant inheritance.