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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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| 主要な著者: | , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Sociedade Brasileira de Dermatologia
2014
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| オンライン･アクセス: | 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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