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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| Autores principales: | , , , , , , , , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
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2023-01-01
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| Colección: | Boletín Médico del Hospital Infantil de México |
| Materias: | |
| Acceso en línea: | https://www.bmhim.com/frame_esp.php?id=352 |
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