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

Abstract Background Rapp-Hodgkin syndrome (RHS) is a rare autosomal dominant disorder caused by TP63 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, accom...

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Hlavní autoři:	Weiai Gan, Jie Wei, Zhengyan Zhao, Ying Zhang, Lan Wu
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	BMC 2026-04-01
Edice:	BMC Oral Health
Témata:	Rapp-Hodgkin Syndrome Leukokeratosis TP63 gene Ectodermal Dysplasia Case Report
On-line přístup:	https://doi.org/10.1186/s12903-026-08478-1
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