Familial ectopic ossification
- PMID: 3126297
- PMCID: PMC1015452
- DOI: 10.1136/jmg.25.2.113
Familial ectopic ossification
Abstract
We report a family with dominantly inherited ectopic ossification. It is characterised by childhood onset of multifocal subcutaneous ossifications (primary osteoma cutis), which are of trivial clinical significance. One family member had extensive ectopic ossification involving one limb. We speculate that this may reflect somatic mutation having caused conversion to homozygosity.
References
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical