The TP63 gene is essential for epithelial proliferation, differentiation, and maintenance during embryogenesis. Despite considerable clinical variability, -related symptoms are characterized by ectodermal dysplasia, distal limb malformations, and orofacial clefts. We identified a novel variant (c.619A > G, p.K207E) in a seven-month-old Chinese patient with orofacial clefts and ectrodactyly but no evident signs of ectodermal dysplasia. This phenotype was rarely reported before. We summarized the presence of the three main -related manifestations in the literature and noted different distributions of CP- and CL/P-related variants regarding p63 structural domains.
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