ArticleJournal of oral and maxillofacial pathology : JOMFP
A rare case report of craniofacial fibrous dysplasia.
Article in Journal of oral and maxillofacial pathology : JOMFP. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed, 12 citations in OpenAlex.
- Polyostotic fibrous dysplasia: Unveiling the complexity of a rare bone disorder through a case report.Radiology case reports · 2025Article
- Fibrous Dysplasia of the Ethmoid Bone Diagnosed in a 10-Year-Old Patient.Medicina (Kaunas, Lithuania) · 2024Article
- Monostotic fibrous dysplasia of jaw bones: a case series.BMC oral health · 2024Article
- Hump on head: Rare case of bi-frontal fibrous dysplasia.Surgical neurology international · 2024Article
- Fibrous Dysplasia Masquerading as Sternal Malignancy: A Rare and Challenging Presentation.Cureus · 2023Article
- [Craniofacial fibrous dysplasia: about six cases].The Pan African medical journal · 2020Article
- Nonspecific Cystic Degeneration in Craniofacial Fibrous Dysplasia: A Rare Finding.Contemporary clinical dentistryArticle
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Authors and funding
4 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Fibrous dysplasia (FD) is a fibro-osseous lesion of the osseous structures of the body. The exact cause is unknown; however, recently, the cause has been reported to be postzygomatic somatic mutation in guanine nucleotide-binding protein, alpha stimulating 1 gene located at chromosome 20q13.2. The three subtypes of FD are monostotic, polyostotic and craniofacial. The term craniofacial FD (CFD) is used to describe FD where the lesions are confined to contiguous bones of the craniofacial skeleton. This report describes the case of CFD of a 20-year-old male patient who had unusual presentation involving right maxilla and frontal bone of the left side of the face. The clinical features, radiological findings and treatment have been discussed.
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