Artlich A, Schwinger E, Meinecke P
Institut für Humangenetik, Medizinische Universität Lübeck, Germany.
Clin Dysmorphol. 1992 Jul;1(3):157-60.
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.
塞特利斯综合征是一种罕见的疾病，主要特征为面部表现，包括双侧颞部类似产钳印记的皮肤改变。有人提出这种独特病症为常染色体隐性遗传。我们报告了一名典型患病的德国男孩，其父亲症状表现则轻得多，由此提示为常染色体显性遗传。
