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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Detalles Bibliográficos
Autores principales: Marques, Gabriela Franco, Tonello, Claudio Sampieri, Sousa, Juliana Martins Prazeres
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Dermatologia 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4056709/
https://www.ncbi.nlm.nih.gov/pubmed/24937825
http://dx.doi.org/10.1590/abd1806-4841.20143043

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4056709/
https://www.ncbi.nlm.nih.gov/pubmed/24937825
http://dx.doi.org/10.1590/abd1806-4841.20143043

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