ReviewJournal of oral biology and craniofacial research
Crouzon syndrome: Genetic and intervention review.
Review in Journal of oral biology and craniofacial research. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 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.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
17 citing papers in PubMed, 41 citations in OpenAlex.
- Article
- Targeted allele-specificMolecular therapy. Nucleic acids · 2025Article
- Ocular manifestations and treatment progress of Crouzon syndrome.International ophthalmology · 2024Review
- Crouzon Syndrome Spanning Three Generations: Advances in the Treatment of Syndromic Midface Deficiency.Plastic and reconstructive surgery. Global open · 2023Article
- Meticulous and Early Understanding of Congenital Cranial Defects Can Save Lives.Children (Basel, Switzerland) · 2023Article
- Crouzon syndrome complicated with binocular strabismus and extraocular muscle fibrosis: a case report.Journal of medical case reports · 2023Article
- A unique presentation of Crouzon-like syndrome: Complex craniosynostosis in the absence of genetic mutations or familial predisposition - A case report.Surgical neurology international · 2023Article
- Crouzon syndrome and the eye: An overview.Indian journal of ophthalmology · 2022Review
- Crouzon syndrome in a fraternal twin: A case report and review of the literature.World journal of clinical cases · 2022Article
- FGFR3 overactivation in the brain is responsible for memory impairments in Crouzon syndrome mouse model.The Journal of experimental medicine · 2022Article
- Computed tomography findings of Crouzon syndrome: A case report.Radiology case reports · 2022Article
- Syndromic Hydrocephalus.Neurosurgery clinics of North America · 2022Review
- Reducing the Burden of Care: Multidisciplinary Management of Late-Manifested Crouzon Syndrome-A Case Report.Children (Basel, Switzerland) · 2021Article
- Extremity anomalies associated with Robinow syndrome.American journal of medical genetics. Part A · 2021Article
- Development and validation of an expanded targeted sequencing panel for non-invasive prenatal diagnosis of sporadic skeletal dysplasia.BMC medical genomics · 2021Article
- Severe craniolacunae and upper and lower extremity anomalies resulting from Crouzon syndrome, FGFR2 mutation, and Ser347Cys variant.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2021Article
- Craniofacial malformations and their association with brain development: the importance of a multidisciplinary approach for treatment.Odontology · 2020Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Crouzon syndrome exhibits considerable phenotypic heterogeneity, in the aetiology of which genetics play an important role.
Indexed as
Identifiers
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.