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Published on: September 8, 2023
Craniofacial Fibrous Dysplasia: Clinical and Therapeutic Implications
Vivian Szymczuk1,2, Jocelyn Taylor1, Alison M Boyce3
1Metabolic Bone Disorders Unit, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD, USA.
Purpose Of Review:
This study aims to review diagnosis, potential complications, and clinical management in craniofacial fibrous dysplasia.
Recent Findings:
Fibrous dysplasia (FD) is a rare mosaic disorder in which normal bone and marrow are replaced with expansile fibro-osseous lesions. Disease presents along a broad spectrum and may be associated with extraskeletal features as part of McCune-Albright syndrome (MAS). The craniofacial skeleton is one of the most commonly impacted areas in FD, and its functional and anatomical complexities create unique challenges for diagnosis and management. This review summarizes current approaches to diagnosis and management in FD/MAS, with emphasis on the clinical and therapeutic implications for the craniofacial skeleton.
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