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

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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Zusammenfassung: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.
ISSN:0275-1879
1754-4505
DOI:10.1111/scd.12236