Syndromic Craniosynostosis: Complexities of Clinical Care | Zendy

Justine O’Hara | Zendy; Federica Ruggiero | Zendy; Louise C. Wilson | Zendy; Greg James | Zendy; Graeme E. Glass | Zendy; Owase Jeelani | Zendy; Juling Ong | Zendy; Richard Bowman | Zendy; Robert Wyatt | Zendy; Robert D. Evans | Zendy; Martin Samuels | Zendy; Richard Hayward | Zendy; David Dunaway | Zendy

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Syndromic Craniosynostosis: Complexities of Clinical Care

Author(s) -

Justine 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

Publication year - 2019

Publication title -

molecular syndromology

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.609

H-Index - 36

eISSN - 1661-8777

pISSN - 1661-8769

DOI - 10.1159/000495739

Subject(s) - craniosynostosis , craniofacial , medicine , multidisciplinary team , presentation (obstetrics) , multidisciplinary approach , craniofacial abnormality , pediatrics , craniosynostoses , craniofacial surgery , synostosis , intensive care medicine , surgery , nursing , social science , psychiatry , sociology

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 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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