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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| Subjects: | |
| Online Access: | Connect to this object online. |
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