Cranio-maxillofacial and dental findings in albright's hereditary osteodystrophy and pseudohypoparathyroidism - Université de Lille Accéder directement au contenu
Article Dans Une Revue The Cleft Palate-Craniofacial Journal Année : 2018

Cranio-maxillofacial and dental findings in albright's hereditary osteodystrophy and pseudohypoparathyroidism

Résumé

The clinical phenotype of pseudohypoparathyroidism (PHP) is caused by Albright's Hereditary Osteodystrophy (AHO). Often, "round face" the only facial clinical sign reported in the literature. The aim of this study was to highlight various cranio-maxillofacial clinical findings associated with AHO. Four patients presented with PHP type 1a. Only one patient exhibited the classical round face. All patients exhibited dental anomalies, class III malocclusion with maxillary retrusion, and a copper beaten appearance of the skull. One suffered from craniosynostosis. The frequency of craniofacial and dental features associated with malocclusion should prompt careful follow-up, particularly during facial growth, in patients with AHO.
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Dates et versions

hal-04475105 , version 1 (23-02-2024)

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Matthias Schlund, Arnaud Depeyre, Florence Kohler, Romain Nicot, Joel Ferri. Cranio-maxillofacial and dental findings in albright's hereditary osteodystrophy and pseudohypoparathyroidism. The Cleft Palate-Craniofacial Journal, 2018, The Cleft Palate-Craniofacial Journal, 56, ⟨10.1177/1055665618814661⟩. ⟨hal-04475105⟩

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