ArticleBMC oral health2019
Craniofacial fibrous dysplasia associated with McCune-Albright syndrome: challenges in diagnosis and treatment: case reports.
Article in BMC oral health, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 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.
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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
10 citing papers in PubMed, 13 citations in OpenAlex.
- Polyostotic fibrous dysplasia: Unveiling the complexity of a rare bone disorder through a case report.Radiology case reports · 2025Article
- Peripheral precocious puberty in girls with McCune-Albright syndrome: a case series.Archives of endocrinology and metabolism · 2025Article
- Fibrous dysplasia in the alveolar crest of edentulous site and the curettage for future implant placement: a case report.BMC oral health · 2025Article
- A novel technique for skull base reconstruction in craniofacial fibrous dysplasia surgery using three-dimensional printing and a dental alginate mold: illustrative case.Journal of neurosurgery. Case lessons · 2024Article
- The Facial Osteoplasty for Polyostotic Fibrous Dysplasia in a Patient With McCune-Albright Syndrome: A Case Report.Cureus · 2023Article
- Diagnosis and treatment of McCune-Albright syndrome: A case report.World journal of clinical cases · 2023Article
- Patient with McCune albright syndrome: Case report and 10 Years of follow-up imaging examination.Journal of clinical and experimental dentistry · 2023Article
- Delayed Diagnosis of McCune-Albright Syndrome.Case reports in genetics · 2021Article
- Imaging of advanced craniofacial fibrous dysplasia associated with McCune-Albright syndrome: A case report.European journal of radiology open · 2020Article
- [Craniofacial fibrous dysplasia: about six cases].The Pan African medical journal · 2020Article
Corrections and comments
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Authors and funding
5 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundMcCune-Albright syndrome (MAS) is a rare multisystem disorder that classically was defined by the triad of polyostotic fibrous dysplasia of bone, café-au-lait skin pigmentation, and precocious puberty. It is a condition that has a gradual onset, slow growth rate and remain painless throughout. The clinical phenotype of MAS is highly variable and no definite treatment is available. CASE PRESENTATION: This article describes two cases, a 10-year-old girl and an 11-year-old boy, both with MAS comprising deforming craniofacial FD. Challenges related to diagnosis and management included late reporting with big lesions, involvement of multiple craniofacial bones, mutilating surgeries and ultimately high degree of morbidity.
conclusionDelayed diagnosis and management of MAS results in devastating physical disabilities and severe morbidity after treatment.
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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.