Rare Association Between Osteogenesis Imperfecta and Chondrosarcoma: Could a Pathogenic Variant in the Gene SERPINF1 Explain It?
Author:
Publisher
Springer Science and Business Media LLC
Subject
Endocrinology,Orthopedics and Sports Medicine,Endocrinology, Diabetes and Metabolism
Link
https://link.springer.com/content/pdf/10.1007/s00223-022-01033-4.pdf
Reference19 articles.
1. Forlino A, Marini JC (2016) Osteogenesis imperfecta. Lancet [Internet]. 387(10028):1657–1671. https://doi.org/10.1016/S0140-6736(15)00728-X
2. Tauer JT, Robinson ME, Rauch F (2019) Osteogenesis imperfecta: new perspectives from clinical and translational research. JBMR Plus 3(8):1–10
3. Trejo P, Palomo T, Montpetit K, Fassier F, Sato A, Glorieux FH et al (2017) Long-term follow-up in osteogenesis imperfecta type VI. Osteoporos Int 28(10):2975–2983
4. Joeng KS, Grover M, Rajagopal A, Lee BH (2014) SERPINF1 as a cause of osteogenesis imperfecta type VI. In: Shapiro JR, Glorieux FH, Byers PH, Sponseller PD (eds) Osteogenesis imperfecta: a translational approach to brittle bone disease. Academic Press, London, pp 167–172
5. Mandziak DG, Clayer M (2013) Chondrosarcoma in a patient with osteogenesis imperfecta. ANZ J Surg 83(10):794–795
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1. Classification of osteogenesis imperfecta: Importance for prophylaxis and genetic counseling;World Journal of Clinical Cases;2023-04-26
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