Spondyloepimetaphyseal dysplasia congenita, Strudwick (medical condition)

An inherited bone growth disorder characterized by short stature, bone abnormalities and vision problems. The bone abnormalities are due to a genetic mutation that affects the development of bone and connective tissue. See also Strudwick syndrome

Chemwatch helps thousands of organisations manage chemical safety. Book a free demo to see how.
Book a Demo →