Fibrodysplasia (myositis) ossificans progressiva (FOP)
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine,Rheumatology
Link
https://link.springer.com/content/pdf/10.1007/s10067-022-06144-9.pdf
Reference7 articles.
1. Shore EM, Xu M, Feldman GJ et al (2006) A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva. Nat Genet 38:525–527
2. Kaplan FS, Al Mukaddam M, Stanley A, Towler OW, Shore EM (2020) Fibrodysplasia ossificans progressiva (FOP): a disorder of osteochondrogenesis. Bone 140:115539
3. De Brasi D, Orlando F, Gaeta V et al (2021) Fibrodysplasia ossificans progressiva: a challenging diagnosis. Genes (Basel) 12:1187. https://doi.org/10.3390/genes12081187
4. Al-Salmi I, Raniga S, Hadidi AA (2014) Fibrodysplasia ossificans progressiva - radiological findings: a case report. Oman Med J 29:368–370
5. Bauer AH, Bonham J, Gutierrez L, Hsiao EC, Motamedi D (2018) Fibrodysplasia ossificans progressiva: a current review of imaging findings. Skeletal Radiol 47:1043–1050
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