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Editorial
. 2022 Jun;41(6):1929-1930.
doi: 10.1007/s10067-022-06144-9. Epub 2022 Mar 28.

Fibrodysplasia (myositis) ossificans progressiva (FOP)

Alfredo Ramirez-Gonzalez  1 , Angelica Castañeda-de-la-Fuente  1 , Vladimir Castro-Cervantes  1 , Carlos Pineda  2 , Hugo Sandoval  2 , Alberto Hidalgo-Bravo  3
Affiliations
Editorial

Fibrodysplasia (myositis) ossificans progressiva (FOP)

Alfredo Ramirez-Gonzalez et al. Clin Rheumatol. 2022 Jun.
No abstract available

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References

    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 - DOI
    1. Kaplan FS, Al Mukaddam M, Stanley A, Towler OW, Shore EM (2020) Fibrodysplasia ossificans progressiva (FOP): a disorder of osteochondrogenesis. Bone 140:115539
    1. 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 - DOI
    1. Al-Salmi I, Raniga S, Hadidi AA (2014) Fibrodysplasia ossificans progressiva - radiological findings: a case report. Oman Med J 29:368–370 - DOI
    1. 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 - DOI

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