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Incontinentia Pigmenti | ||
| Iranian Journal of Medical Sciences | ||
| مقاله 19، دوره 26، 3-4، اسفند 2001، صفحه 178-181 اصل مقاله (777.7 K) | ||
| نوع مقاله: Case Report(s) | ||
| نویسندگان | ||
| G. Faghihi* ؛ F. Iraji | ||
| Department of Dermatology, Isfahan University of Medical Sciences, Isfahan | ||
| چکیده | ||
| Incontinentia pigmenti (IP) is an uncommon X-linked dominant genodermatosis characterized by four cutaneous stages and frequent association with dental (90%), central nervous system (33%) and ocular (35%) anomalies. The exact pathogenesis of this disorder remains unknown.Herein, we report a newborn girl with inflammatory vesiculobullous and warty skin lesions and a positive family history of IP, with blood leucocytosis (eosinophilia and also lymphocytosis), but no other extracutaneous findings. | ||
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