Fibrodysplasia Ossificans Progressiva in a 23-Year-Old Male.

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Date
2014-05
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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.
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Keywords
Fibrodysplasia Ossificans Progressiva (FOP), Autosomal dominant, Bony exostosis
Citation
Al-Mustaque Ahmed, Montasir Ahmed Al, Amin Mashah Binte. Fibrodysplasia Ossificans Progressiva in a 23-Year-Old Male. Journal of Enam Medical College. 2014 May; 4(2): 126-129.