Blepharo-cheilo-dontic (BCD) syndrome: Report on four new patients

dc.contributorUniversidade de São Paulo (USP)
dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T13:25:39Z
dc.date.accessioned2022-10-05T13:17:13Z
dc.date.available2014-05-20T13:25:39Z
dc.date.available2022-10-05T13:17:13Z
dc.date.created2014-05-20T13:25:39Z
dc.date.issued1998-03-05
dc.identifierAmerican Journal of Medical Genetics. New York: Wiley-liss, v. 76, n. 2, p. 133-136, 1998.
dc.identifier0148-7299
dc.identifierhttp://hdl.handle.net/11449/8161
dc.identifier10.1002/(SICI)1096-8628(19980305)76:2<133
dc.identifierWOS:000072258700005
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3884851
dc.description.abstractWe report on four Brazilian patients with, among other signs, cleft lip and palate, dental anomalies, ectropion of the lower eyelids, euryblepharon, and lagophthalmia, Two were sporadic cases and two were familial cases, a mother and her equally affected son, Recently, the reports with different combination of these signs were reviewed by Gorlin et al, [1996; Am J Med Genet 65:109-112] and named blepharo-cheilo-dontic (BCD) syndrome, Variable expressivity and autosomal dominant inheritance were observed. (C) 1998 Wiley-Liss, Inc.
dc.languageeng
dc.publisherWiley-Blackwell
dc.relationAmerican Journal of Medical Genetics
dc.rightsAcesso restrito
dc.sourceWeb of Science
dc.subjectfacial clefting
dc.subjectdental anomaly
dc.subjectectropion
dc.subjecteuryblepharon
dc.subjectlagophthalmia
dc.subjectankyloblepharon
dc.titleBlepharo-cheilo-dontic (BCD) syndrome: Report on four new patients
dc.typeArtigo


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