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: Daniela de Almeida Figueiras (Author), Deborah Maria de Castro Barbosa Leal (Author), Valter Kozmhinsky (Author), Marina Coutinho Domingues Querino (Author), Marina Genesia da Silva Regueira (Author), Maria Gabriela de Morais Studart (Author)
Format: Book
Published: Sociedade Brasileira de Dermatologia, 2016-10-01T00:00:00Z.
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