Ocular colobomata, polydactyly, cleft palate and panhypopituitarism: a new syndrome

Abstract

We describe a male patient with ocular colobomata, cleft palate, polydactyly, panhypopituitarism and possible craniosynostosis, whom we have followed for 30 years. Although there are some similarities to other documented syndromes, this previously unreported combination of features appears to constitute a new syndrome.