TY - CHAP M1 - Book, Section TI - Familial Progressive Scleroderma A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - Disorder characterized by progressive systemic sclerosis (scleroderma), calcium deposits (calcinosis) usually in the fingers, Raynaud Syndrome, loss of muscle control of the esophagus (difficult swallowing), osseous deformity of the fingers (sclerodactyly), and small red spots (telangiectasia) on the skin (fingers, face) or inside the mouth. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/28 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=1164069705 ER -