Crouzon Syndrome: Visual Diagnosis
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference10 articles.
1. Etiopathogenesis of craniosynostosis;Cohen;Neurosurgery Clinics of North America,1991
2. Paternal origin of FGFR2 mutations in sporadic cases of Crouzon syndrome and Pfeiffer syndrome;Glaser;American Journal of Human Genetics,2000
3. Difficulties of delayed treatment of craniosynostosis in a patient with Crouzon, increased intracranial pressure, and papilledema;Kirman;Journal of Craniofacial Surgery,2011
4. Evidence-based approach for making cochlear implant recommendations for infants with residual hearing loss;Leigh;Ear and Hearing,2011
5. Dental rehabilitation in a patient with Crouzon's syndrome: A case report;Maloth;International Journal of Dental Case Reports,2012
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1. 3D computer-aided single stage correction of Crouzon related craniofacial and occlusal deformities: A case series of three adult patients;Oral and Maxillofacial Surgery Cases;2024-03
2. The Effect of Yes-Associated Protein on the Interaction Between the MEK/Extracellular Signal-Regulated Kinase and Hippo Pathways in Osteoblasts Co-Cultured With Fibroblast Growth Factor Receptor 2-Mutated Dura Cells;Journal of Craniofacial Surgery;2021-09-13
3. Clinical assessment and FGFR2 mutation analysis in a Chinese family with Crouzon syndrome;Medicine;2021-03-12
4. What is your diagnosis?;Journal of the Turkish-German Gynecological Association;2020-09-01
5. Detection of G338R FGFR2 mutation in a Vietnamese patient with Crouzon syndrome;Biomedical Reports;2019-01-03
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