The Greig polysyndactyly craniofacial dysmorphism syndrome: variable expression in a family
- PMID: 6262085
- DOI: 10.1007/BF00441928
The Greig polysyndactyly craniofacial dysmorphism syndrome: variable expression in a family
Abstract
A severe expression of the Greig polysyndactyly-craniofacial dysmorphism syndrome is reported in two dizygotic 4-month-old twin brothers. A minor expression of this autosomal dominant syndrome was present in the father.