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Autosomal dominant osteosclerosis, Worth type
rareA sclerozing bone disorder characterized by generalized skeletal densification, particularly of the cranial vault and tubular long bones, which is not associated to an increased risk of fracture.
- Identifiers
- MONDO:0007764 OMIM:144750OMIM:607636Orphanet:2790
- Causal genes
- LRP5
- Part of
- HyperostosisSkeletal dysplasia
- Also known as
- endosteal hyperostosis, Worth type · hyperostosis corticalis generalisata, benign form of Worth with torus palatinus · hyperostosis, endosteal · osteosclerosis of the skull and enlarged mandible · osteosclerosis, autosomal dominant, Worth type
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