TY - CHAP M1 - Book, Section TI - Krieble-Bixler Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - It is an inherited medical condition characterized by craniofacial area and skeletal abnormalities. The clinical features include craniosynostosis, prominent forehead, midface hypoplasia, proptosis and ocular hypotelorism, submucosal cleft palate, radiohumeral or radioulnar dysostosis, arachnodactyly, particularly a clinodactyly of the fifth finger, and hypospadias. It may present with tetralogy of Fallot and short stature (dwarfism). SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/29 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164075949 ER -