Resumen

GONZALEZ BURGOS, Lourdes et al. Bloch-Sulzberger's syndrome (Incontinentia pigmenti): Contribution with a case report. Arch. argent. pediatr. [online]. 2011, vol.109, n.3, pp.e62-e65. ISSN 0325-0075.

Incontinentia pigmenti (IP) is a rare genodermatosis. Skin lesions, that are present in all patients affected, evolve in stages. The frst is the erythematous blistering stage, wich differential diagnosis includes a wide variety of diseases. We present a case of a female neonate with blisters present at birth, where the skin biopsy confirmed the diagnosis of IP.

Palabras clave : Genodermatosis; Incontinentia pigmenti; Bloch-Sulzberger's syndrome.

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