TY - CHAP M1 - Book, Section TI - Dubowitz Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - Genetic disorder with craniofacial (craniosynostosis), neurologic, orthopedic, and dermatologic anomalies. The clinical features include short stature, failure to thrive, microencephaly, micrognathia, retrognathia, mild intellectual disabilities, and eczema. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/29 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164068391 ER -