Article
Clinical and histologic features of incontinentia pigmenti in adults with nuclear factor-κB essential modulator gene mutations.
Journal of the American Academy of Dermatology - 1 Mar 2011
Hadj-Rabia Smaïl, Rimella Aude, Smahi Asma, Fraitag Sylvie, Hamel-Teillac Dominique, Bonnefont Jean-Paul, de Prost Yves, Bodemer Christine
Abstract excerpt
BACKGROUND: Incontinentia pigmenti (IP) is a multisystem disorder, in which cutaneous symptoms can be accompanied by dental, ocular, and central nervous system defects. In adults, the clinical diagnosis of IP is based principally on the late onset of stage 4 lesions and their association with dental, nail, ocular, or central nervous system anomalies. Nevertheless, these lesions are often unrecognized. OBJECTIVES:...
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