The terminal period findings of late-diagnosed fibrodysplasia ossificans progressiva

Fibrodysplasia ossificans progressiva (FOP) is an autosomal dominant rare disease characterized by foot deformities and concomitant heterotopic ossifications. Theoretically, in the absence of early diagnosis and medication, the patient’s outcome will be poor. The patients are usually diagnosed at an...

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Detalles Bibliográficos
Autores principales: Doğan, Emrah, Aydoğmuş, Hüseyin, Elibol, Cenk, Aydoğmuş, Sinem
Formato: Online Artículo Texto
Lenguaje:English
Publicado: German Medical Science GMS Publishing House 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10436734/
https://www.ncbi.nlm.nih.gov/pubmed/37599859
http://dx.doi.org/10.3205/000326

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10436734/
https://www.ncbi.nlm.nih.gov/pubmed/37599859
http://dx.doi.org/10.3205/000326

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