“…In addition to these findings, some of the affected patients were also reported to present nail changes, peri-and subungeal keratoses, follicular hyperkeratosis, hyperhidrosis, and oral keratotic lesions at other points of mechanical pressure. [1][2][3][4] Since the first description of focal palmoplantar and gingival keratosis (FPGK) in 1964, 2 only a few cases have been reported, including some families affected by the disease in several consecutive generations pointing to autosomal dominant inheritance. 1,[3][4][5][6] The clinical features of the disease remain to be defined in more detail.…”