Syndromic Craniosynostosis: Complexities of Clinical Care
2019; Karger Publishers; Volume: 10; Issue: 1-2 Linguagem: Inglês
10.1159/000495739
ISSN1661-8777
AutoresJustine O’Hara, Federica Ruggiero, Louise C. Wilson, Greg James, Graeme E. Glass, Owase Jeelani, Juling Ong, Richard Bowman, Robert Wyatt, Robert D. Evans, Martin Samuels, Richard Hayward, David Dunaway,
Tópico(s)dental development and anomalies
ResumoPatients 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 aims to marry genotypic and phenotypic knowledge with clinical presentation and management of the craniofacial syndromes presenting most frequently to the craniofacial unit at Great Ormond Street Hospital for Children NHS Foundation Trust.
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