Fibrodysplasia ossificans progressiva or Munchmeyer's disease: A rare case report

Fibrodysplasia ossificans progressiva (FOP) is a rare autosomal dominant disease. It is characterized by widespread soft tissue ossification and congenital stigmata of the extremities, affecting all ethnic backgrounds. The worldwide reported prevalence is approximately 1/2,000,000. Based on history...

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Detalles Bibliográficos
Autores principales: Bhansali, Sonal Priya, Tiwari, Anjali Dave, Mittal, Sankalp, Pareek, Sitaram, Nasir, Iram
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8191566/
https://www.ncbi.nlm.nih.gov/pubmed/34188414
http://dx.doi.org/10.4103/njms.NJMS_52_19

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8191566/
https://www.ncbi.nlm.nih.gov/pubmed/34188414
http://dx.doi.org/10.4103/njms.NJMS_52_19

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