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Apert’s Syndrome: Report of a New Case and its Management
In this article, an interesting case of Apert syndrome in a 14-year-old boy with characteristic craniosynostosis, acrocephaly, midface hypoplasia, pharyngeal attenuation, ocular manifestations, and syndactyly of the hands and feet is presented. The case is discussed in the light of relevant literatu...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Jaypee Brothers Medical Publishers
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4086543/ https://ncbi.nlm.nih.gov/pubmed/25206089 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5005/jp-journals-10005-1009 |
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