4.5 Article

Fibrodysplasia ossificans progressiva in Hong Kong-A case report series

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FRONTIERS IN PEDIATRICS
卷 11, 期 -, 页码 -

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FRONTIERS MEDIA SA
DOI: 10.3389/fped.2023.1152731

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case report; fibrodysplasia ossificans progressiva; ACVR1; Hong Kong; FOP

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Fibrodysplasia ossificans progressiva (FOP) is a rare condition with challenging diagnosis due to its rarity and non-specific symptoms. Early diagnosis and suitable management are crucial for preserving patients' function and quality of life. This report shares the diagnostic journeys and clinical courses of 8 FOP patients in Hong Kong, highlighting the associated challenges.
Fibrodysplasia ossificans progressiva (FOP) is an ultra-rare condition. The diagnosis could be challenging due to its rarity and non-specific presenting symptoms. However, early diagnosis and appropriate management help in preserving patients' function and quality of life. Herein, we report the diagnostic journeys and clinical courses of 8 patients with FOP in Hong Kong and illustrate the challenges involved.

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