Fibrodysplasia Ossificans Progressiva: Difficulty in Diagnosis and Management A case report and literature review

INTRODUCTION: Fibrodysplasia ossificans progressiva (FOP) is a rare autosomal dominant genetic disorder and characterized by postnatal progressive heterotopic ossification of the connective tissue. There are difficulties in diagnosing FOP, thus delayed or misdiagnosis and mismanagement is common. 3D...

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Detalles Bibliográficos
Autores principales: Kamal, Achmad Fauzi, Novriansyah, Robin, Rahyussalim, Prabowo, Yogi, Siregar, Nurjati Chairani
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Indian Orthopaedic Research Group 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4719346/
https://www.ncbi.nlm.nih.gov/pubmed/27299014
http://dx.doi.org/10.13107/jocr.2250-0685.248

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4719346/
https://www.ncbi.nlm.nih.gov/pubmed/27299014
http://dx.doi.org/10.13107/jocr.2250-0685.248

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