Syndromic Craniosynostosis: Complexities of Clinical Care

Patients with syndromic craniosynostosis have a molecularly identified genetic cause for the premature closure of their cranial sutures and associated facial and extra-cranial features. Their clinical complexity demands comprehensive management by an extensive multidisciplinary team. This review aim...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Mol Syndromol
Prif Awduron: O'Hara, Justine, Ruggiero, Federica, Wilson, Louise, James, Greg, Glass, Graeme, Jeelani, Owase, Ong, Juling, Bowman, Richard, Wyatt, Michelle, Evans, Robert, Samuels, Martin, Hayward, Richard, Dunaway, David J.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: S. Karger AG 2019
Pynciau:
Review Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC6422147/
https://ncbi.nlm.nih.gov/pubmed/30976282
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000495739
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