RANK‐L inhibitor as a promising agent for refractory extensive craniofacial fibrous dysplasia: A case report

Background McCune‐Albright syndrome is a rare disorder characterized by polyostotic fibrous dysplasia (FD), café‐au‐lait skin pigmentation, and endocrine dysfunction. Extensive FD in the craniofacial region can present significant challenges in terms of disease control and carries a high risk of per...

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Veröffentlicht in:	Head & neck 2024-01, Vol.46 (1), p.E1-E5
Hauptverfasser:	Abouammo, Moataz D., Alsavaf, Mohammad Bilal, Prevedello, Daniel M., Ghalib, Luma, Boyce, Alison M., Carrau, Ricardo L.
Format:	Artikel
Sprache:	eng
Schlagworte:	craniofacial denosumab Disease control Fibrous dysplasia Humanities and Social Sciences McCune‐Albright syndrome optic decompression Optic nerve Pigmentation Skin pigmentation
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