Niemann-Seyde S C, Eber S W, Zoll B
Institut für Humangenetik, Universität Göttingen, FRG.
Clin Genet. 1991 Oct;40(4):271-6. doi: 10.1111/j.1399-0004.1991.tb03095.x.
The acrocephalosyndactylies (ACS) are a group of inherited disorders characterized by premature fusion of cranial sutures in association with abnormalities of the hands and feet. Based on their clinical features, different types of ACS have been described. We here report on a family with 9 individuals affected with ACS III (Saethre-Chotzen syndrome), 5 of them severely. Clinical features of the patients are presented with regard to differential diagnostic delineations.
尖头并指(趾)畸形(ACS)是一组遗传性疾病,其特征是颅缝过早融合并伴有手足异常。根据临床特征,已描述了不同类型的ACS。我们在此报告一个有9名成员患III型ACS(塞特勒-乔岑综合征)的家系,其中5人病情严重。针对鉴别诊断,介绍了患者的临床特征。