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Unilateral Coronal Craniosynostosis in an Apert-Like Patient
BACKGROUND AND SIGNIFICANCE: Apert syndrome is a congenital disorder of patients who typically present with bilateral coronal craniosynostosis and varying degrees of complex syndactyly of the hands and feet, among other features. We describe a unique presentation of a rare Apert-like patient with un...
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| Publicado no: | Plast Surg (Oakv) |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
SAGE Publications
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6399773/ https://ncbi.nlm.nih.gov/pubmed/30854365 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/2292550318800322 |
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