A Case of Fibrodysplasia Ossificans Progressiva in a 5-year-old Boy with all Musculoskeletal Features and Review of the Literature

INTRODUCTION: Fibrodysplasia ossificans progressiva previously known as myositis ossificans progressiva is a rare connective tissue disorder with autosomal dominant genetic inheritance. Patients develop heterotrophic ossification starting with the first decade of life. Diagnosis is extremely difficu...

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Detalles Bibliográficos
Autores principales: Civan, Melih, Bilgili, Fuat, Kilic, Ayse, Uyguner, ZeyraOya, Toksoy, Guven
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Indian Orthopaedic Research Group 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6367301/
https://www.ncbi.nlm.nih.gov/pubmed/30740372
http://dx.doi.org/10.13107/jocr.2250-0685.1200

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6367301/
https://www.ncbi.nlm.nih.gov/pubmed/30740372
http://dx.doi.org/10.13107/jocr.2250-0685.1200

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