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Syndrome of a craniofacial dysostosis, limb malformation, and omphalocele
R J Gardner1, P S Morrison, L A Faigan
1Department of Paediatrics and Child Health, University of Otago, Dunedin, New Zealand.
American Journal of Medical Genetics
|June 1, 1990
Abstract:
We describe an infant with a unique combination of a severe craniofacial dysostosis and a very distinctive facies, severe limb defects, a thoracic deformity, and an omphalocele as the major anomalies. We propose that this represents a "new" syndrome of multiple congenital abnormalities.