Fibrodysplasia Ossificans Progressiva in a 23-Year-Old Male

Authors

  • Ahmed Al-Mustaque Assistant Professor, Department of Orthopedics, TMSS Medical College, Bogra
  • Ahmed Al Montasir Resident Physician, Department of Medicine, Rafatullah Community Hospital, Bogra
  • Mashah Binte Amin Consultant, Department of Radiology & Imaging, Abeda Memorial Hospital, Tongi, Dhaka

DOI:

https://doi.org/10.3329/jemc.v4i2.19682

Keywords:

Fibrodysplasia Ossificans Progressiva (FOP), Autosomal dominant, Bony exostosis

Abstract

Fibrodysplasia Ossificans Progressiva (FOP) is an inherited disease in which progressive ossification of striated muscles, tendons, ligaments and other connective tissues forming bridges of extra bones across the joints leads to severe disability and there are associated characteristic congenital skeletal malformations. FOP is also known as Stoneman's syndrome. The case we report here is a 23-year-old male with the clinical and radiologic characteristics of FOP.

DOI: http://dx.doi.org/10.3329/jemc.v4i2.19682

J Enam Med Col 2014; 4(2): 126-129

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Published

2014-07-24

How to Cite

Al-Mustaque, A., Al Montasir, A., & Amin, M. B. (2014). Fibrodysplasia Ossificans Progressiva in a 23-Year-Old Male. Journal of Enam Medical College, 4(2), 126–129. https://doi.org/10.3329/jemc.v4i2.19682

Issue

Vol. 4 No. 2 (2014)

Section

Case Reports

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