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Fibrous dysplasia
rareA genetic, non-inheritable disorder caused by osteoblastic differentiation defects that result in the replacement of bone marrow and trabecular bone by fibrous stroma and immature bone. It usually affects a single bone and less frequently multiple bones. Skull, femur, tibia, and humerus are the most frequently affected bones. It manifests with pain, deformities, and fractures.
- Identifiers
- MONDO:0000845 Orphanet:249
- Also known as
- fibrous dysplasia of bone
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