| Literature DB >> 2222925 |
K H Chranowska1, M Krajewska-Walasek, Z Rump, L Wisniewski, J P Fryns.
Abstract
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.Entities:
Mesh:
Year: 1990 PMID: 2222925
Source DB: PubMed Journal: Genet Couns ISSN: 1015-8146