RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164078508 T1 Metaphyseal Chondrodysplasia, Jansen Type T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e YR 2019 FD 2019 PB McGraw-Hill Education PP New York, NY SN 9781259861789 LK accessanesthesiology.mhmedical.com/content.aspx?aid=1164078508 RD 2024/03/29 AB It is an extremely rare progressive disorder in which portions of the bones of the arms and legs develop abnormally with unusual cartilage formations and subsequent abnormal bulbous metaphyses, ie, metaphyseal chondrodysplasia deformations. Affected individuals exhibit unusually short-limbed dwarfism. The onset of the disease becomes apparent typically during early childhood. Infants with Jansen-Type Metaphyseal Chondrodysplasia may have characteristic facial abnormalities and additional skeletal malformations. Hypercalcemia is present.