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

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dc.contributor.authorAl-Mustaque, Ahmed
dc.contributor.authorMontasir, Ahmed Al
dc.contributor.authorAmin, Mashah Binte
dc.date.accessioned2016-02-15T11:24:11Z
dc.date.available2016-02-15T11:24:11Z
dc.date.issued2014-05
dc.description.abstractFibrodysplasia 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.en_US
dc.identifier.citationAl-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.en_US
dc.identifier.issn2227-6688
dc.identifier.issn2304-9316
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/172928
dc.language.isoenen_US
dc.source.urihttps://www.banglajol.info/index.php/JEMC/article/view/19682en_US
dc.subjectFibrodysplasia Ossificans Progressiva (FOP)en_US
dc.subjectAutosomal dominanten_US
dc.subjectBony exostosisen_US
dc.titleFibrodysplasia Ossificans Progressiva in a 23-Year-Old Male.en_US
dc.typeArticleen_US
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