Title of article
Incontinentia pigmenti: a newborn with characteristic skin lesions and bilateral optic atrophy: case report and review of literature.
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 ,
Issue Information
ماهنامه با شماره پیاپی 0 سال 2013
Pages
6
From page
805
To page
810
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.
Journal title
Acta Medica Iranica
Serial Year
2013
Journal title
Acta Medica Iranica
Record number
2386186
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