Grant syndrome

Grant syndrome is a rare osteogenesis imperfecta-like disorder, described in two patients to date, characterized clinically by persistent wormian bones, blue sclera, mandibular hypoplasia, shallow glenoid fossa, and campomelia. There have been no further descriptions in the literature since 1986.

Also known as: Grant syndrome, persistent wormian bones, blue sclerae, mandibular hypoplasia, shallow glenoid fossae and campomelia

0 clinical trials for this condition and its sub-types, 0 tagged with Grant syndrome itself.