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Incontinentia pigmenti or Bloch-Sulzberger syndrome: a rare X-linked genodermatosis()

Incontinentia pigmenti is a rare X-linked genodermatosis that affects mainly female neonates. The first manifestation occurs in the early neonatal period and progresses through four stages: vesicular, verruciform, hyperpigmented and hypopigmented. Clinical features also manifest themselves through c...

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Autori principali: Marques, Gabriela Franco, Tonello, Claudio Sampieri, Sousa, Juliana Martins Prazeres
Natura: Artigo
Lingua:Inglês
Pubblicazione: Sociedade Brasileira de Dermatologia 2014
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4056709/
https://ncbi.nlm.nih.gov/pubmed/24937825
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1590/abd1806-4841.20143043
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