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Incontinentia Pigmenti: A Newborn with Characteristic Skin Lesions and Bilateral Optic Atrophy: Case Report and Review of Literature
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نویسنده
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Azizzadeh Maryam ,Rezaei Morteza ,Hashemi Nargess
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منبع
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acta medica iranica - 2013 - دوره : 51 - شماره : 11 - صفحه:805 -810
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چکیده
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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.
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کلیدواژه
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Bloch- Sulzberger disease; Incontinentia Pigmenti; Optic atrophy; Newborn
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آدرس
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semnan university of medical sciences, Department of Dermatology, ایران, semnan university of medical sciences, Department of Pediatrics, ایران, semnan university of medical sciences, Department of Pediatrics, ایران
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پست الکترونیکی
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hashemin553@yahoo.com
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Authors
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