Merlob P, Grünebaum M, Reisner S H
Acta Paediatr Scand. 1981 Mar;70(2):275-7. doi: 10.1111/j.1651-2227.1981.tb05557.x.
A newborn infant with craniofacial dysmorphism and polysndactyly (Greig's Syndrome) is reported. This syndrome is manifested by postaxial polydactyly of the fingers and preaxial polydactyly of the toes, with syndactyly. The craniofacial dysmorphism is characterized by frontal bossing and other variable manifestations. X-ray examination revealed markedly advanced bone age. The mode of inheritance appears to be autosomal dominant.
报告了一名患有颅面畸形和多指(Greig综合征)的新生儿。该综合征表现为手指轴后多指和脚趾轴前多指,并伴有并指。颅面畸形的特征为前额突出及其他多种表现。X线检查显示骨龄明显超前。遗传方式似乎为常染色体显性遗传。