Pfeiffer syndrome: oral healthcare management and description of new dental findings in a craniosynostosis

ABSTRACTPfeiffer syndrome is a rare fibroblast growth factor receptor‐related craniosynostosis with variable clinical presentations. We describe new dental findings of hypodontia, microdontia, dilacerations, and radicular dentin dysplasia in a 19‐year‐old girl, and discuss the oral health management...

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Veröffentlicht in:	Special care in dentistry 2017-09, Vol.37 (5), p.258-262
Hauptverfasser:	Hassona, Yazan, Al‐Hadidi, Abeer, Ghlassi, Thaer Abu, Dali, Hanin El, Scully, Crispian
Format:	Artikel
Sprache:	eng
Schlagworte:	Acrocephalosyndactylia - diagnosis Consanguinity Cranial sutures Craniosynostosis dental anomalies Dentin dentine dysplasia Dentistry Dysplasia Female Fibroblast growth factors Heart Defects, Congenital - diagnosis Humans Oral hygiene Pediatrics Pedigree Pfeiffer Phenotype Stomatognathic System Abnormalities - etiology Stomatognathic System Abnormalities - therapy Young Adult
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