Oculoectodermal syndrome: twentieth described case with new manifestations
Abstract Oculoectodermal syndrome is a rare disease characterized by the association of aplasia cutis congenita, epibulbar dermoids, and other abnormalities. This report describes the twentieth case of the disease. We report a 4-year-old female child who presented with the classical features of the...
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Main Authors: | , , , , , |
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Format: | Book |
Published: |
Sociedade Brasileira de Dermatologia,
2016-10-01T00:00:00Z.
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Connect to this object online.3rd Floor Main Library
Call Number: |
A1234.567 |
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Copy 1 | Available |