Resumen

LEITAO, Cátia Vilas Boas et al. Dermatology clinical case. Nascer e Crescer [online]. 2021, vol.30, n.1, pp.61-63.  Epub 31-Ene-2021. ISSN 0872-0754.  https://doi.org/10.25753/birthgrowthmj.v30.i1.18674.

Incontinentia pigmenti is an X-linked neuroectodermal dysplasia. It is a rare genetic disease with multiorgan involvement, and hence a multidisciplinary approach is of paramount importance. Although diagnosis is based on clinical findings, genetic molecular testing can be performed to confirm diagnosis and allow future genetic counselling.

The authors describe the case of a 4-month-old girl accidentally diagnosed with incontinentia pigmenti following routine physical examination in the Emergency Department. Timely diagnosis enabled appropriate multidisciplinary approach and follow-up.

Palabras clave : Blaschko lines; genodermatoses; incontinentia pigmenti; rare disease.

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