Incontinentia pigmenti (Bloch-Sulzberger syndrome): a case report.

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dc.contributor.authorNiccoli-Filho, W. D.
dc.contributor.authorda Rocha, J. C.
dc.contributor.authorDi Nicoló, R.
dc.contributor.authorSeraidarian, P. I.
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-27T11:17:53Z
dc.date.available2014-05-27T11:17:53Z
dc.date.issued1993-06-01
dc.description.abstractA syndrome--incontinentia pigmenti--of probable genetic etiology, is discussed and a new case report presented. The syndrome presents systemic and dental manifestations, which are separate although similar to those found in other disease entities, i.e., congenital syphilis, hereditary ectodermal dysplasia.en
dc.format.extent251-253
dc.identifier.citationThe Journal of clinical pediatric dentistry, v. 17, n. 4, p. 251-253, 1993.
dc.identifier.issn1053-4628
dc.identifier.lattes4153738182937249
dc.identifier.orcid0000-0001-9132-0429
dc.identifier.scopus2-s2.0-0027613490
dc.identifier.urihttp://hdl.handle.net/11449/64380
dc.language.isoeng
dc.relation.ispartofThe Journal of clinical pediatric dentistry
dc.relation.ispartofjcr0.854
dc.relation.ispartofsjr0,469
dc.rights.accessRightsAcesso restrito
dc.sourceScopus
dc.subjectcase report
dc.subjectchild
dc.subjectfemale
dc.subjecthuman
dc.subjectincontinentia pigmenti
dc.subjectpathology
dc.subjectpathophysiology
dc.subjectsex difference
dc.subjecttooth eruption
dc.subjecttooth malformation
dc.subjectCase Report
dc.subjectChild
dc.subjectFemale
dc.subjectHuman
dc.subjectIncontinentia Pigmenti
dc.subjectSex Factors
dc.subjectTooth Abnormalities
dc.subjectTooth Eruption
dc.titleIncontinentia pigmenti (Bloch-Sulzberger syndrome): a case report.en
dc.typeArtigo
unesp.author.lattes4153738182937249[3]
unesp.author.orcid0000-0001-9132-0429[3]

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