Case Reports
doi: 10.1001/archpedi.1979.02130080058010.
Greig cephalopolysyndactyly syndrome
- PMID: 223435
- DOI: 10.1001/archpedi.1979.02130080058010
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Case Reports
Greig cephalopolysyndactyly syndrome
Am J Dis Child.
1979 Aug.
Abstract
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.
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