Fibrodysplasia Ossificans Progressiva: Literature Review and Case Report
Background. Fibrodysplasia ossificans progressiva (FOP) is a genetic disease of the heterotopic ossification group associated with the mutation in ACVR1/ALK2 gene. FOP is characterized by progressive heterotopic endochondral ossification of connective tissue that occurs in postnatal period. It leads...
Main Authors: | , , , |
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Format: | Article |
Language: | English |
Published: |
"Paediatrician" Publishers LLC
2023-01-01
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Series: | Вопросы современной педиатрии |
Subjects: | |
Online Access: | https://vsp.spr-journal.ru/jour/article/view/3069 |