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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/52294
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dc.contributor.authorLaforest, C.-
dc.contributor.authorLeibovitch, I.-
dc.contributor.authorSelva-Nayagam, D.-
dc.contributor.authorCrompton, J.-
dc.contributor.authorHaan, E.-
dc.date.issued2008-
dc.identifier.citationClinical Dysmorphology, 2008; 17(2):87-90-
dc.identifier.issn0962-8827-
dc.identifier.issn1473-5717-
dc.identifier.urihttp://hdl.handle.net/2440/52294-
dc.description.abstractWe 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.-
dc.description.statementofresponsibilityLaforest, Caroline; Leibovitch, Igal; Selva, Dinesh; Crompton, John; Haan, Eric-
dc.language.isoen-
dc.publisherLippincott Williams & Wilkins-
dc.source.urihttp://dx.doi.org/10.1097/01.mcd.0000228427.79358.0b-
dc.subjectHumans-
dc.subjectCleft Palate-
dc.subjectPolydactyly-
dc.subjectHypopituitarism-
dc.subjectColoboma-
dc.subjectAbnormalities, Multiple-
dc.subjectSyndrome-
dc.subjectFacies-
dc.subjectAdult-
dc.subjectMale-
dc.titleOcular colobomata, polydactyly, cleft palate and panhypopituitarism: a new syndrome-
dc.typeJournal article-
dc.identifier.doi10.1097/01.mcd.0000228427.79358.0b-
pubs.publication-statusPublished-
dc.identifier.orcidSelva-Nayagam, D. [0000-0002-2169-5417]-
dc.identifier.orcidHaan, E. [0000-0002-7310-5124]-
Appears in Collections:Aurora harvest 5
Paediatrics publications

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