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Apert Syndrome: Late presentation and treatment challenges
Apert syndrome is a rare autosomal dominant disorder characterized by craniosynostosis, craniofacial anomalies, and severe symmetrical syndactyly of the hands and feet. Anomalies of the viscera, skeleton and cardiovascular system have also been reported… Untreated craniosynostosis leads to inhibitio...
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| Yayımlandı: | Sudan J Paediatr |
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| Asıl Yazarlar: | , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Sudanese Association of Pediatricians
2014
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4949801/ https://ncbi.nlm.nih.gov/pubmed/27493407 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/sjp-14-71 |
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