RT Journal
A1 Duncan PA, Klein RM, Wilmot PL, Shapiro LR
T1 GReig cephalopolysyndactyly syndrome
JF American Journal of Diseases of Children
JO American Journal of Diseases of Children
YR 1979
FD August 1
VO 133
IS 8
SP 818
OP 821
DO 10.1001/archpedi.1979.02130080058010
UL http://dx.doi.org/10.1001/archpedi.1979.02130080058010
AB • Based on the family presented and five others previously described, it can be concluded that the Grieg cephalopolysyndactyly syndrome is a fully penetrant autosomal dominant disease consisting of four variably expressed malformations: postaxial polydactyly (type B), preaxial polydactyly, syndactyly, and minor craniofacial abnormalities. This entity can be differentiated from other craniofacial-digital syndromes because of the absence of mental retardation, craniosynostosis, and brachydactyly.(Am J Dis Child 133:818-821, 1979)