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

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dc.contributor.authorMaarouf, Sarah
dc.contributor.authorClark, Marie
dc.contributor.authorChen, Anthony
dc.contributor.authorHaggstrom, Anita
dc.date.accessioned2025-07-11T13:58:42Z
dc.date.available2025-07-11T13:58:42Z
dc.date.issued2024-07-26
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.identifier.citationMaarouf S, Clark M, Chen A, Haggstrom A. Dental Abnormalities in Congenital Ichthyoses: Case Report and Review of the Literature. Poster presented at: Indiana University Medical Student Program for Research and Scholarship (IMPRS) Research Symposium; July 25-26, 2024; Indianapolis, IN.
dc.identifier.urihttps://hdl.handle.net/1805/49355
dc.language.isoen_US
dc.relation.isversionof10.1111/pde.15841
dc.rightsAttribution 4.0 Internationalen
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectcongenital
dc.subjectectodermal dysplasia
dc.subjectichthyosis
dc.subjectnatal teeth
dc.subjecttooth abnormalities
dc.subjectneonatal diseases and abnormalities
dc.titleDental Abnormalities in Congenital Ichthyoses: Case Report and Review of the Literature
dc.typePoster
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