Four new cases of incontinentia pigmenti are presented, including chromosome studies of one family. An increased number of chromosome breakages was found in the blood of affected as well as unaffected members of this family.

Case presentation of staged surgical treatment of patients with spinal deformity in incontinentia pigmenti syndrome. As a result of surgical procedure proper sagittal balance of the body was restored.

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 u...

Incontinentia pigmenti is a rare, dominantly X-linked genodermatosis characterized by multisystemic involvement that is lethal prenatally in the majority of affected males and shows great clinical variability when it is expressed in women. Recently it has been shown that mutations of the gene NEMO/IKK-g located in Xq28 cause the expression of the disease, being only one mutation responsible for...

Incontinentia pigmenti is an uncommon type of ectodermal dyspIasia involving abnormalities of the skin, hair, central nervous system, and teeth. The literature is reviewed and a case with a variety of dental abnormalities is presented. Incontinentia pigrnenti (IP) is one of the lesser known ectodermal dysplasias with fewer than 800 cases reported in the world literature. This genodermatosis aff...