ListarGI-UDISAP - Artigos por tema "Acrocefalosindactilia Tipo I"
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Síndrome de Apert: tratamiento ortopédico
(UCM, 2011)[Abstract] Apert syndrome is an autosomal dominant disorder characterized by craniosynostosis, midfacial malformations and symmetric syndactyly of hands and feet. We present a case of a female Caucasian, 45 years old, ...