Resumen

SANTOS, Sónia et al. Incontinentia pigmenti: a case report. Nascer e Crescer [online]. 2012, vol.21, n.2, pp.99-101. ISSN 0872-0754.

Introduction: Incontinentia pigmenti (IP) is a rare genodermatosis neuroectodermal multisystem disorder. This disease has an incidence of 1:50.000 births and is typically lethal in males, in utero. Case report: The authors present a clinical case of IP in a newborn with papulovesiculous eruptions observed on the first day of life. The evolution, anatomopathology and genetic study findings established the diagnosis. Conclusion: The IP is a potentially serious clinical entity, which requires an early diagnosis and multidisciplinary follow-up.

Palabras clave : Incontinentia pigmenti; newborn; papulovesiculous eruptions.

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