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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| Main Authors: | , , |
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| Format: | Book |
| Published: |
Sociedade Brasileira de Dermatologia,
2014-06-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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Connect to this object online.3rd Floor Main Library
| Call Number: |
A1234.567 |
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| Copy 1 | Available |