a multidisciplinary approach to a seven year-old patient with incontinentia pigmenti: a case report and five-year follow up

incontinentia pigmenti is a rare inherited disorder involving abnormalities of the skin, hair, eyes, musculoskeletal system, central nervous system, and the teeth. dental abnormalities are the most common manifestations of this disorder. the purpose of this case report was to present the clinical and radiological findings of a seven-year-old girl as well as the results of her five-year follow up. the patient showed faded linear pigmented macular lesions on the trunk and on upper and lower limbs. dental examination was notable for conical and peg-shaped anterior teeth as well as delayed eruption of primary and permanent teeth. in addition to conservative treatments, prosthetic treatments such as interim removable partial dentures were indicated for the patient. keywords: incontinentia pigmenti; dental prosthesis; genetic diseases, inborn