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Apert syndrome: A case report and review of the literature
Apert syndrome is the rare acrocephalosyndactyly syndrome type 1, characterized by craniosynostosis, severe syndactyly of hands and feet, and dysmorphic facial features. It demonstrates autosomal dominant inheritance assigned to mutations in the fibroblast growth factor receptor gene. Presently desc...
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| Publicado no: | North Clin Istanb |
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| Autor principal: | |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Kare Publishing
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5206464/ https://ncbi.nlm.nih.gov/pubmed/28058401 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.14744/nci.2015.30602 |
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