Olmsted Syndrome a Rare Type of Mutilating Palmoplantar Keratoderma: A Case Report
Abstract Olmsted syndrome is a rare genetic disease characterized by mutilating transgradient palmoplantar keratoderma (PPK) associated with periorificial keratotic plaques. Its starts in the neonatal period or in childhood. The disease has a slow but progressive and extremely disabling course. We present a case with clinically and pathologically confirmed Olmsted syndrome. This case report is an important one for its rarity and disability. Keywords: JAK inhibitors, Alopecia Areata |