Fibrodysplasia Ossificans Progressiva – A Rare Genetic Disorder and the Role of Technetium-99m Methylene Diphosphonate Bone Scan

Fibrodysplasia ossificans progressiva is a rare genetic disease believed to occur in approximately 1 in 2 million people worldwide and is characterized by progressive extraosseous ossification over the course of a lifetime in an inevitable and unpredictable episodic manner, with most patients being...

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Detalles Bibliográficos
Autores principales: Gupta, Nitin, Pruthi, Ankur, Kumar, Suneel, Verma, Ritu, Belho, Ethel Shangne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2019
Materias:
Case Series
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6593934/
https://www.ncbi.nlm.nih.gov/pubmed/31293300
http://dx.doi.org/10.4103/ijnm.IJNM_57_19

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6593934/
https://www.ncbi.nlm.nih.gov/pubmed/31293300
http://dx.doi.org/10.4103/ijnm.IJNM_57_19

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