TY - CHAP M1 - Book, Section TI - Grant Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e 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. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/29 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164071578 ER -