Bianchi E, Aricŏ M, Podestă A F, Grana M, Fiori P, Beluffi G
Am J Med Genet. 1985 Dec;22(4):649-58. doi: 10.1002/ajmg.1320220402.
Acrocephalosyndactyly (ACS) is an inherited syndrome of premature synostosis of the cranial sutures and abnormalities in the distal segments of the limbs. Several forms of ACS have been described. ACS type III (or Saethre-Chotzen syndrome) is characterized by microcephaly, skull asymmetry, mild syndactyly, and facial abnormalities. We describe an Italian family with ACS III in which two sibs are clearly affected; the mother and the maternal grandmother show some features of the syndrome.
尖头并指(趾)畸形(ACS)是一种颅缝过早闭合和肢体远端节段异常的遗传性综合征。已描述了几种ACS类型。III型ACS(或塞特雷-乔岑综合征)的特征是小头畸形、颅骨不对称、轻度并指(趾)畸形和面部异常。我们描述了一个患有III型ACS的意大利家庭,其中两个同胞明显患病;母亲和外祖母表现出该综合征的一些特征。