Clinical Features, Diagnosis and Management of Fibrodysplasia Ossificans Progressiva / 罕见病研究
JOURNAL OF RARE DISEASES
; (4): 501-508, 2023.
Article
in Zh
| WPRIM
| ID: wpr-1004925
Responsible library:
WPRO
ABSTRACT
Fibrodysplasia ossificans progressiva(FOP) is a rare congenital disease characterized by progressive heterotopic ossification, causing severe immobility with multi-system involvement. The relatively low incidence rate and incomplete knowledge among clinicians of the disease often result in misuse of invasive procedures or surgical treatment, leading to the progression of heterotopic ossification. To promote the knowledge of FOP, this article presents a comprehensive review involving epidemiology, pathological mechanisms, clinical features, diagnosis, and management of the FOP.
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Index:
WPRIM
Language:
Zh
Journal:
JOURNAL OF RARE DISEASES
Year:
2023
Type:
Article