Fibrodysplasie ossifiante progressive (FOP) à propos d’un cas
DOI:
https://doi.org/10.55715/jaim.v17i2.781Keywords:
Fibrodysplasia ossificans progressiva, standard x-ray.Abstract
Fibrodysplasia ossificans progressiva (FOP) or myositis ossificans is an extremely rare progressive genetic disease that affects one in a million people. The mode of transmission of FOP is autosomal dominant, with no association with race, sex or geographic distribution. We report a case of fibrodysplasia ossificans progressiva (FOP) or myositis ossificans in a 5-year-old patient admitted for suspected multiple exostoses disease. The clinical examination revealed limited joint mobility of the spine, shoulders, elbows and a skeletal deformation in the craniocaudal and proximo-distal directions. The diagnosis of FOP had been suggested by the typical appearances on standard skeletal radiography. The patient had received treatment with corticosteroids and anti-inflammatories. The course was punctuated by episodes of flare-ups and remissions followed by death in a picture of cardio-respiratory distress.
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This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License. Copyright @2017. This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License (http://creativecommons.org/licenses/by-nc-sa/4.0/) which permits unrestricted non-commercial used, distribution and reproduction in any medium
