Síndrome de Apert: relato de dois casos e revisão de literatura
Apert's syndrome is the type I acrocephalosyndactyly. It was described by Apert, and is characterized by craniosynostosis with fusion of the cranial sutures and / or its base, associated with maxillary hypoplasy, symmetrical syndactyly of hands and feet and other systemic malformations. Mental de...
| Autor principal: | ALENCAR, Lecidio da Silva |
|---|---|
| Outros Autores: | BAROSEIRO, Paula Jorgiane Leitão Diniz |
| Grau: | Trabalho de Conclusão de Curso - Graduação |
| Publicado em: |
2022
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| Assuntos: | |
| Acesso em linha: |
https://bdm.ufpa.br:8443/jspui/handle/prefix/4801 |