21 Chapter Chapter Chapter Chapter Chapter Chapter Chapter Chapter Chapter Chapter Chapter 1 2 3 4 5 6 7 8 9 10 11 16. Gooijer K, Harsevoort AGJ, van Dijk FS, Withaar H, Janus GJM, Franken AAM. A Baseline Measurement of Quality of Life in 322 Adults With Osteogenesis Imperfecta. JBMR Plus 2020; 4. DOI:10.1002/jbm4.10416. 17. Van Dijk FS, Cobben JM, Kariminejad A, et al. Osteogenesis imperfecta: A review with clinical examples. Mol Syndromol 2011; 2. DOI:10.1159/000332228. 18. Bilo RAC, Robben SGF, Van Rijn RR, Maat GJR, Huls NM. Forensic aspects of paediatric fractures: Differentiating accidental trauma from child abuse. 2010 DOI:10.1007/978-3-54078716-7. 19. Ablin DS, Greenspan A, Reinhart M, Grix A. Differentiation of child abuse from osteogenesis imperfecta. American Journal of Roentgenology 1990; 154. DOI:10.2214/ajr.154.5.2108539. 20. Marlowe A, Pepin MG, Byers PH. Testing for osteogenesis imperfecta in cases of suspected non-accidental injury. J Med Genet 2002; 39. DOI:10.1136/jmg.39.6.382. 21. Evereklioglu C, Madenci E, Bayazit YA, Yilmaz K, Balat A, Bekir NA. Central corneal thickness is lower in osteogenesis imperfecta and negatively correlates with the presence of blue sclera. Ophthalmic and Physiological Optics 2002; 22. DOI:10.1046/j.1475-1313.2002.00062.x. 22. Chan CC, Green WR, Cruz ZC, Hillis A. Ocular Findings in Osteogenesis Imperfecta Congenita. Archives of Ophthalmology 1982; 100. DOI:10.1001/archopht.1982.01030040437014. 23. Lanting PJH, Borsboom PCF, Meerman GJ te, Kate LP ten. Decreased scattering coefficient of blue sclerae. Clin Genet 1985; 27. DOI:10.1111/j.1399-0004.1985.tb00209.x. 24. Chau FY, Wallace D, Vajaranant T, et al. Osteogenesis Imperfecta and the Eye. In: Osteogenesis Imperfecta: A Translational Approach to Brittle Bone Disease. 2013. DOI:10.1016/B9780-12-397165-4.00031-9. 25. Viswanathan D, Goldberg I, Graham SL. Relationship of change in central corneal thickness to visual field progression in eyes with glaucoma. Graefe’s Archive for Clinical and Experimental Ophthalmology 2013; 251. DOI:10.1007/s00417-013-2295-6. 26. Luder HU, Van Waes H, Raghunath M, Steinmann B. Mild dental findings associated with severe osteogenesis imperfecta due to a point mutation in the α2(I)) collagen gene demonstrate different expression of the genetic defect in bone and teeth. J Craniofac Genet Dev Biol 1996; 16. 27. Lindau B, Dietz W, Lundgren T, Storhaug K, Rgen JÈ, Nore G. Discrimination of morphological findings in dentine from osteogenesis imperfecta patients using combinations of polarized light microscopy, microradiograhpy and scanning electron microscopy. Int J Paediatr Dent 1999; 9: 253–61.
RkJQdWJsaXNoZXIy MTk4NDMw