Ectodermal dysplasia, ectrodactyly, clefting, anophthalmia microphthalmia, and genitourinary anomalies: nosology of goltz-gorlin syndrome versus eec syndrome

dc.contributorUniversidade de São Paulo (USP)
dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T15:23:39Z
dc.date.available2014-05-20T15:23:39Z
dc.date.created2014-05-20T15:23:39Z
dc.date.issued1992-02-01
dc.identifierAmerican Journal of Medical Genetics. New York: Wiley-liss, v. 42, n. 3, p. 276-280, 1992.
dc.identifier0148-7299
dc.identifierhttp://hdl.handle.net/11449/34404
dc.identifier10.1002/ajmg.1320420303
dc.identifierWOS:A1992HA73700002
dc.description.abstractWe report on two unrelated Brazilian girls born to normal and nonconsanguineous parents and presenting ectodermal dysplasia, ectrodactyly, clefting, tear duct anomalies, and micro/anophthalmia. The clinical picture presented by these patients suggests the diagnosis of Goltz-Gorlin (Focal dermal hypoplasia) syndrome and EEC syndrome.
dc.languageeng
dc.publisherWiley-Blackwell
dc.relationAmerican Journal of Medical Genetics
dc.rightsAcesso restrito
dc.sourceWeb of Science
dc.subjectMCA MALFORMATION SYNDROMES
dc.subjectX-LINKED INHERITANCE
dc.subjectGOLTZ-GORLIN SYNDROME
dc.titleEctodermal dysplasia, ectrodactyly, clefting, anophthalmia microphthalmia, and genitourinary anomalies: nosology of goltz-gorlin syndrome versus eec syndrome
dc.typeArtículos de revistas


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