Management of A Patient with Kindler Syndrome: A Case Report

Abstract Kindler syndrome is an uncommon autosomal recessive condition marked by the presence of bullae on the extremities in infants, progressive changes in skin pigmentation and texture (poikiloderma), thinning of the skin, sensitivity to sunlight, as well as various issues affecting mucous membranes and increased fragility of the gums. This report presents the case of two siblings who were Asian male, showcasing the critical appearance of skin and oral manifestations of kindlers syndrome followed by conservative management of both cases.