RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164071578 T1 Grant Syndrome T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e YR 2019 FD 2019 PB McGraw-Hill Education PP New York, NY SN 9781259861789 LK accesspediatrics.mhmedical.com/content.aspx?aid=1164071578 RD 2024/03/29 AB Grant Syndrome is a rare osteogenesis imperfecta-like disorder. It is characterized clinically by the presence of persistent wormian bones, blue sclerae, mandibular hypoplasia, shallow glenoid fossa, and camptomelia. Other clinical features include hypotonic musculature at birth, bilateral wrist dislocations, and femoral and tibial bowing.