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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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Bibliographic Details
Published in:Sudan J Paediatr
Main Authors: Kheir, Abdelmoneim E M, Hamed, Ahlam A, Maki, Wala M, Hasan, Lina H M
Format: Artigo
Language:Inglês
Published: Sudanese Association of Pediatricians 2014
Subjects:
Online Access: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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