Condition report · Musculoskeletal
An inherited condition in which fibrous tissue replaces bone in the lower and upper jaw during childhood, giving rounded cheeks; it usually stabilises or improves after puberty.
A condition report looks for rare variants known to cause the conditions it covers.
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What your report covers
Autosomal dominant
Bilateral painless swelling of the jaws from early childhood due to fibrous lesions, caused by variants in SH3BP2; teeth may be displaced or lost.
Genes analysed
Also known as
CRBM; familial fibrous dysplasia of the jaws; familial multilocular cystic disease of the jaws
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