Article

A case of Rapp-Hodgkin syndrome featuring prominent oral leukokeratosis linked to a TP63 gene variant

2026-03-10

Abstract excerpt

<title>Abstract</title> <p> <bold>Background:</bold> Rapp-Hodgkin syndrome (RHS) is a rare autosomal dominant disorder caused by <italic>TP63</italic> gene mutations. This case warrants reporting due to the presence of significant limb malformations, extensive caries in the maxillary teeth, and congenital absence of multiple mandibular teeth, accompanied by remarkably widespread oral leukokeratosis. Its novel...

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Literature Corpus work: 45c28666-24af-5996-9d90-20fba25cd282
DOI: 10.21203/rs.3.rs-8632040/v1

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