Fibrodysplasia ossificans progressiva in a 3-year-old female patient

Background: Fibrodysplasia ossificans progressiva (FOP) is a rare autosomal dominant disease affecting connective tissue, primarily caused by de novo mutations of the ACVR1 gene. FOP is a disease with congenital malformations of the toes and heterotopic ossification in characteristic patterns that p...

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Autors principals:	Cecilia Moreira, Gabriel Dapueto, Gabriel Peluffo, Alejandra Vomero, Alejandra Tapié, Soledad Rodríguez, Victor Raggio, Rodrigo Suárez, Gustavo Giachetto, Loreley García
Format:	Artigo
Idioma:	Inglês
Publicat:	Permanyer 2023-01-01
Col·lecció:	Boletín Médico del Hospital Infantil de México
Matèries:	Myositis ossificans. ACVR1 gene. Hallux valgus.
Accés en línia:	https://www.bmhim.com/frame_esp.php?id=352
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