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  • Title: Setleis (bitemporal 'forceps marks') syndrome in a German family: evidence for autosomal dominant inheritance.
    Author: Artlich A, Schwinger E, Meinecke P.
    Journal: Clin Dysmorphol; 1992 Jul; 1(3):157-60. PubMed ID: 1342863.
    Abstract:
    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.
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