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- E R Tonholo-Silva, E A Adachi, M S Tafner, and L Yoshinaga.
- Department of Pediatrics, Faculdade de Medicina de Marília (FMM), SP, Brasil.
- Arq Neuropsiquiatr. 1994 Mar 1; 52 (1): 100-2.
AbstractFibrodysplasia (myositis) ossificans progressiva (FOP) is a rare autosomal dominant disorder in which there is a progressive ectopic ossification and skeletal malformation, mainly in the connective tissue of muscle. The diagnosis is based on the clinical findings and radiological demonstration of the skeletal malformations. We report a 5 year-old female case with FOP.
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