Incontinentia pigmenti: a newborn with characteristic skin lesions and bilateral optic atrophy: case report and review of literature.
作者： Maryam Azizzadeh , Nargess Hashemi , Morteza Rezaei
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摘要: 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 estimated that there have been nearly 900-1200 affected individuals. In this article, literature reviewed case of IP characteristic skin lesions optic atrophy presented.
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