Familial ossifying fibroma

Orpha code: 435329OMIM code: 137575

Definition

A rare genetic bone disease characterized by multifocal, painless, benign fibrocemento-osseous lesions of the jaws which expand progressively and can cause severe facial deformity. It usually manifests at an early age and is often associated with abnormalities of the long bones and pathologic fractures. Radiologically, the lesions are of mixed radiopaque/radiolucent appearance. Incomplete surgical removal may lead to more rapid growth of the residual lesion.

Disease data
Classification

Disease

Synonyms
Multiple ossifying fibroma
Familial Gigantiform cementoma
Multiple ossifying fibroma
ORPHA code
435329
OMIM code
137575
ICD10 code
D16.4
ICD11 code
-

No additional description.

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