We report five patients from two different pedigrees with the ectrodactyly-ectodermal dysplasia-clefting syndrome (EEC). All had features of ectodermal dysplasia, but only three had limb ectrodactyly and orofacial clefting. The present patients illustrate the great phenotypic variability in the EEC syndrome. As no single feature, including any of the three cardinal signs, is mandatory for syndrome diagnosis, a meticulous examination of all family members is needed.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1046/j.1525-1470.2003.20203.x | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!