Fibrodysplasia Ossificans Progressiva: Literature Review and Case Report

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...

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Bibliographic Details
Main Authors: Natalya N. Korableva, Evgeniy V. Berestnev, Sergey M. Kiselyov, Natalya F. Chipsanova
Format: Article
Language:English
Published: "Paediatrician" Publishers LLC 2023-01-01
Series:Вопросы современной педиатрии
Subjects:
клинический случай
фибродисплазия оссифицирующая прогрессирующая
оссифицирующий миозит
орфанные заболевания
гетеротопическая оссификация
ревматология
Online Access:https://vsp.spr-journal.ru/jour/article/view/3069

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