Chranowska K H, Krajewska-Walasek M, Rump Z, Wisniewski L, Fryns J P
Department of Human Genetics, Child Health-Centre Memorial Hospital, Warsaw.
Genet Couns. 1990;1(1):67-73.
In this report we present another family with oligosymptomatic expression of the EEC syndrome. A mother with complete absence of the permanent teeth had two children with split hand/split foot deformity, as typically seen in the EEC syndrome. Cleft lip/cleft palate was also present in one of them. The great variability in expression of this autosomal dominant syndrome is discussed and the difficulties in genetic counseling are emphasized.
在本报告中,我们介绍了另一例EEC综合征表现为症状较少的家族病例。一位恒牙完全缺失的母亲育有两个孩子,他们患有典型的EEC综合征所具有的并指/并趾畸形。其中一个孩子还患有唇腭裂。本文讨论了这种常染色体显性综合征表现的巨大变异性,并强调了遗传咨询中的困难。