Dental Abnormalities in Congenital Ichthyoses: Case Report and Review of the Literature

dc.contributor.authorMaarouf, Sarah
dc.contributor.authorClark, Marie
dc.contributor.authorChen, Anthony
dc.contributor.authorHaggstrom, Anita
dc.contributor.departmentDermatology, School of Medicine
dc.date.accessioned2025-04-22T08:53:21Z
dc.date.available2025-04-22T08:53:21Z
dc.date.issued2025
dc.description.abstractWe describe a 1-day old female with features of keratitis-ichthyosis-deafness (KID) syndrome and natal teeth. Genetic analysis confirmed GJB2 263C and A88V de novo pathogenic variants consistent with KID syndrome. Natal teeth were promptly extracted to avoid the risk of aspiration. This review describes subsets of ichthyoses that have been reported in association with dental anomalies, highlighting the need for early dental referral and importance of long-term follow-up.
dc.eprint.versionFinal published version
dc.identifier.citationMaarouf S, Clark M, Chen A, Haggstrom A. Dental Abnormalities in Congenital Ichthyoses: Case Report and Review of the Literature. Pediatr Dermatol. 2025;42(2):305-310. doi:10.1111/pde.15841
dc.identifier.urihttps://hdl.handle.net/1805/47262
dc.language.isoen_US
dc.publisherWiley
dc.relation.isversionof10.1111/pde.15841
dc.relation.journalPediatric Dermatology
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internationalen
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourcePMC
dc.subjectCongenital
dc.subjectEctodermal dysplasia
dc.subjectHereditary
dc.subjectIchthyosis
dc.subjectNatal teeth
dc.subjectNeonatal diseases and abnormalities
dc.subjectTooth abnormalities
dc.titleDental Abnormalities in Congenital Ichthyoses: Case Report and Review of the Literature
dc.typeArticle
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