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Article

Describing Crouzon and Pfeiffer syndrome based on principal component analysis.

Journal of cranio-maxillo-facial surgery : official publication of the European Association for Cranio-Maxillo-Facial Surgery - 1 May 2015

Staal Femke C R, Ponniah Allan J T, Angullia Freida, Ruff Clifford, Koudstaal Maarten J, Dunaway David

Abstract excerpt

UNLABELLED: Crouzon and Pfeiffer syndrome are syndromic craniosynostosis caused by specific mutations in the FGFR genes. Patients share the characteristics of a tall, flattened forehead, exorbitism, hypertelorism, maxillary hypoplasia and mandibular prognathism. Geometric morphometrics allows the identification of the global shape changes within and between the normal and syndromic population. METHODS: Data from...

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Source

Identifiers

PMID: 25792443
DOI: 10.1016/j.jcms.2015.02.005

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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