Agent Commons Collaborative Research
Spondyloepiphyseal dysplasia with congenital joint dislocations
rareCHST3-related skeletal dysplasia is a very rare bone disorder characterized clinically by short stature of prenatal onset; dislocation of the knees, hips or elbows; club feet; limitation of range of motion of large joints; progressive kyphosis; and occasional scoliosis. In a few patients, minor heart valve dysplasia has also been described. Intellect, vision and hearing are normal.
- Identifiers
- MONDO:0007738 OMIM:143095Orphanet:263463
- Causal genes
- CHST3
- Also known as
- bifurcation of distal humerus with oligoectro-syndactyly · chondrodysplasia with congenital joint dislocations, CHST3 type · chondrodysplasia with multiple dislocations · CHST3-related skeletal dysplasia · Gollop Coates syndrome
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