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...

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Detalles Bibliográficos
Publicado en:Mol Syndromol
Autores principales: 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.
Formato: Artigo
Lenguaje:Inglês
Publicado: S. Karger AG 2019
Materias:
Review Article
Acceso en línea: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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