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recessive Robinow syndrome
Pathology:
- skeletal dysplasia
Genetics:
- associated with defects in ROR2
Clinical manifestations:
- generalized limb bone shortening
- segmental defects of the spine
- brachydactyly
- dysmorphic facial appearance
General
genetic syndrome (multisystem disorder)
Database Correlations
OMIM 268310
References
OMIM :accession 268310