Author/Authors :
Azizzadeh، Maryam نويسنده Kowsar Hospital, School of Medicine, Semnan University of Medical Sciences, Semnan, IR Iran , , Rezaei-Zadeh، Morteza نويسنده , , HASHEMI، Nargess نويسنده Department of Pediatric Neurology, Ghaem Medical Center, Mashhad University of Medical Sciences, Mashhad, Iran ,
Abstract :
Incontinentia Pigmenti (IP) is a rare X-linked dominant disorder with skin, eye, central nervous system (CNS) and tooth abnormalities. According to the reported cases, it is estimated that there have been nearly 900-1200 affected individuals. In this article, the literature is reviewed and a case of IP with characteristic skin lesions and optic atrophy is presented.
