| Literature DB >> 2124774 |
L Bruni1, P Giammaria, M C Tozzi, D Camparcola, F Scopinaro, C Imperato.
Abstract
Fibrodysplasia ossificans progressiva (FOP) is a severe, rare, autosomal dominant, ectopic ossifying condition, with primary involvement of the skeletal muscles associated with skeletal abnormalities. This report concerns an 11-year-old boy suffering from FOP, who presented significant modification of the musculoskeletal structure of the thorax and problems with articular movements. The patient showed progress after treatment with ethane-1-hydroxy-1,1-diphosphonate (EHDP). In fact, using a scintiscanner we were able to observe a significant improvement in symptoms and a recovery of some of the active sites of ossification.Entities:
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Year: 1990 PMID: 2124774 DOI: 10.1111/j.1651-2227.1990.tb11371.x
Source DB: PubMed Journal: Acta Paediatr Scand ISSN: 0001-656X