RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164072251 T1 Hecht 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=1164072251 RD 2024/11/01 AB Rare, inherited disorder, characterized by trismus and pseudocamptodactyly. This medical condition called “Trismus-pseudocamptodactyly Syndrome” is a disorder characterized by short muscles and tendons resulting in limited range of motion of the hands, legs, and mouth. The most serious complication includes the limited opening of the mouth, a very serious considerations in anesthesia.