GuidelineOrphanet journal of rare diseases2012
Clinical guidelines for the management of craniofacial fibrous dysplasia.
Guideline in Orphanet journal of rare diseases, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 112 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
112 citing papers in PubMed, 315 citations in OpenAlex.
- Benign Sinonasal Tumors: A 17-Year Single Center Experience.Turkish archives of otorhinolaryngology · 2026Article
- Intensive, interdisciplinary pain treatment in fibrous dysplasia/McCune-Albright syndrome.JBMR plus · 2026Article
- Fibrous Dysplasia Presenting as an Exophytic Gingival Mass: A Rare Clinical Presentation.Journal of clinical medicine · 2026Article
- Endoscopic Endonasal Resection of Fibro-Osseous Lesions Involving the Nasal Turbinates: A Report of Two Cases and a Literature Review.Journal of rhinology : official journal of the Korean Rhinologic Society · 2026Article
- Bilateral Lesions Are Linked to Postoperative Regrowth in Craniofacial Fibrous Dysplasia: Alkaline Phosphatase as a Marker of Clinical Phenotype.Diagnostics (Basel, Switzerland) · 2026Article
- A Cemented Total Hip Arthroplasty Without Osteotomy for Severe Femoral Deformity in Fibrous Dysplasia: A Case Report.Cureus · 2026Article
- Decompression Surgery in Bilateral Compressive Optic Neuropathy Secondary to Vitamin A Deficiency.Neuro-ophthalmology (Aeolus Press) · 2026Article
- Fibrous dysplasia of the jaws: four cases with conservative and resective surgical management.Case reports in plastic surgery & hand surgery · 2026Article
- Case Report: Total hip arthroplasty via the direct anterior approach using a cementless revision stem without corrective osteotomy for fibrous dysplasia.Frontiers in surgery · 2026Article
- McCune-Albright Syndrome: A Case Series.Cureus · 2026Article
- A Rare Case of Mandibular Chondrosarcoma Arising from Fibrous Dysplasia.Dentistry journal · 2025Article
- Craniofacial fibrous dysplasia: a challenge for general dental practitioners.British dental journal · 2025Article
- Injury-induced niche factors Cxcl12 and Shh/Ihh coordinate suture stem cell activation during calvarial bone regeneration.Science signaling · 2025Article
- Article
- Developing a Standardised Dataset for Natural History Studies in Fibrous Dysplasia/McCune-Albright Syndrome.Calcified tissue international · 2025Article
- Integration of Clinical, Radiographic, Histologic, and Molecular Findings to Diagnose Craniofacial Fibrous Dysplasia.The Journal of craniofacial surgery · 2025Article
- Article
- Clival fibrous dysplasia in which short interval disease progression posed a diagnostic challenge in a skeletally mature patient: a case report.Journal of medical case reports · 2025Article
- Two-stage surgical strategy for extensive craniofacial fibrous dysplasia with cerebral compression.Acta neurochirurgica · 2025Article
- Imaging of the skull base and orbital tumors.Japanese journal of radiology · 2025Review
52 more citing papers are in PubMed but not listed here.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors at 7 institutions in 2 countries.
Funding
Abstract
Fibrous dysplasia (FD) is a non-malignant condition caused by post-zygotic, activating mutations of the GNAS gene that results in inhibition of the differentiation and proliferation of bone-forming stromal cells and leads to the replacement of normal bone and marrow by fibrous tissue and woven bone. The phenotype is variable and may be isolated to a single skeletal site or multiple sites and sometimes is associated with extraskeletal manifestations in the skin and/or endocrine organs (McCune-Albright syndrome). The clinical behavior and progression of FD may also vary, thereby making the management of this condition difficult with few established clinical guidelines. This paper provides a clinically-focused comprehensive description of craniofacial FD, its natural progression, the components of the diagnostic evaluation and the multi-disciplinary management, and considerations for future research.
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What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.